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*  Montgomery Area School District
Mechanical Device Tax/Per Device $125, a real estate transfer tax 0.5%, coupled with substantial funding from the Commonwealth ... 89 school districts received approval to exceed the Index in full while others received a partial approval of their request. ... while others received a partial approval of their request. For special education costs, 119 districts received approval to ... while others received a partial approval of their request. For special education costs, 104 districts received approval to ...
*  Delay box
... electronic nitrous oxide injection controllers and other devices. Delay box manufacturers that do not receive NHRA approval are ... Only a few delay box manufacturers were willing to pay NHRA delay box approval fees and submit designs for the NHRA's approval ... The NHRA also began requiring delay box manufacturers to pay a fee and submit delay box designs for the NHRA's approval. Then ... Once submitted for NHRA approval, and paying the fee, delay box manufactures were not allowed to make any changes in design for ...
*  Reporting Body Identifier
... codes indicate the following approval/allocation bodies: Normally, when a RBI is 35, the phone device supports operation on the ... a given mobile device, and allocated the model a unique code. The numbers are loosely based on the telephone country code (CC) ... of the organization identified, as most approving nations used a single approval body endorsed by their national GSM ...
*  Kfar Malal
... for a device that assesses left ventricular systolic dysfunction (LVSD). The device aids physicians in detecting heart failure ... In 2009, NI Medical, a biotech company located in Kfar Malal, received approval by the U.S. Food and Drug Administration (FDA) ... 11 January 2014 Germany's EuroHypo bank to refinance Park Azorim British Israel Asymptomatic HF detection device receives FDA ...
*  Y. Pierre Gobin
The device was conceived in 1995 after a frustrating experience in the operating room in which surgeons were unable to reopen a ... received FDA approval in 2004. In 2001, Gobin became professor of radiology in neurosurgery and neurology at the Weill Cornell ... The device, which by then had been named the Mechanical Embolus Removal in Cerebral Ischemia, or MERCI for short, ... At UCLA, Gobin was part of the team that invented an new device to remove blood clots from the brain, which cause ischemic ...
*  California Proposition 65 (1986)
"Electronic Devices". Archived from the original on 2007-10-29. "California Hotel & Lodging Association Helps Lodging Guests ... resulting in the requirement of the Attorney General's approval of pre-trial Proposition 65 settlements. The Attorney General ... Understand Proposition 65; Court Approval Obtained for Comprehensive Compliance Procedure" (Press release). California Hotel & ...
*  SYNCTHINK
"Virtual Reality Medical Devices : SyncThink Eye-Sync". Trendhunter.com. Retrieved 2016-04-25. "EYE-SYNC Device That Assesses ... "SyncThink Gains FDA Approval for EYE-SYNC". Vrnewsblog.wordpress.com. 2016-03-22. Retrieved 2016-04-25. " ... SyncThink sells its diagnostic device under the EYE-SYNC label. The EYE-SYNC is a high-performance device that uses virtual ... The EYE-SYNC received FDA clearance in January, 2016 to market the technology as a medical device. The device is currently used ...
*  Drug recall
Apropos to medical devices, private for-profit firms were allowed to review the products instead of the FDA. The 21st Century ... In 2015, 45 new drugs were passed by the FDA, which is more than double than the approval rate 10 years ago. The 21st Century ... Drugs and medical devices are typically recalled if the product is defective, contaminated, contains a foreign object, fails to ... Medical device safety alerts occur when there are unreasonable safety risks associated with using a product. A more ...
*  Camilo R. Gomez
Katz, JM; Gobin YP (May 2006). "Merci Retriever in acute stroke treatment". Expert Rev Med Devices. 3 (3): 273-280. doi:10.1586 ... work on mechanical neuroendovascular rescue of acute ischemic stroke preceded all the work that led to the more recent approval ... Solitaire and Trevo Pro devices. In the early 1990s he coined the phrase Time is Brain!, as an argument for the need to ... by the U.S. Food and Drug Administration (FDA) of devices specifically designed for this purpose, including the MERCI Retriever ...
*  Laboratory Developed Test
FDA will allow these products to enter the market without prior approval from the Agency. On July 31, 2014, the FDA announced ... has determined that while such tests qualify as medical devices, ...
*  Yossi Gross
... the FDA Ophthalmic Devices Advisory Panel voted 8-0 to approve, with conditions including post-approval studies, the premarket ... He spoke at the American Israel Chamber meeting on the topic: Accelerating Medical Device Start-ups the Israeli Way and at the ... From the late 1990s through 2007, Gross launched 27 separate medical device companies, all based on his patents and inventions ... "Accelerating Medical Device Start-ups the Israeli Way". "Future Shock Diane McManus, Jewish Exponent Feature". "David Cassak, " ...
*  American Institute for Medical and Biological Engineering
Bringing with them medical devices and technologies, Fellows illustrate how federal investments in bioengineering research and ... to regulatory approval by FDA. AIMBE hosts an annual Congressional Lunch Briefing Series to inform Congress and the public on ... AIMBE was one of the first organizations to partner with the Center for Devices and Radiological Health (CDRH) at FDA to sign a ... and the regulatory processes that governs the medical device sector; and (3) Train rising leaders in the field to learn first- ...
*  Bird scarer
Ultrasonic devices are static sound-emitting bird deterrents, which, in theory, will annoy birds to keep them away from ... In the United Kingdom the use of balloons is subject to approval from the Civil Aviation Authority, especially around airfields ... A bird scarer is any of a number devices designed to scare birds, usually employed by farmers to dissuade birds from eating ... The scarecrow idea has been built upon numerous times, and not all visual scare devices are shaped like humans. The "Flashman ...
*  Jack Zigler
It was the second device to be approved by the FDA for such a purpose. As a condition of approval, Synthes Spine is required to ... The study will include the 286 patients who participated in the pre-approval clinical trials. The company is also required to ... PhD Quoted on Raleigh-Durham ABC affiliate's website discussing nonfusion surgical devices Zigler is a contributing eEditor to ...
*  Thermo Electron
In April 2007, Genevac was sold to Riverlake Partners LLC and the merger closed with FTC approval. Zetatron, a high-voltage ... vacuum tube device that generates a stream of neutrons http://web.mit.edu/newsoffice/founders/Thermo.html Company founding ...
*  Personal transporter
... personal technical device/medium) for "personal transporter with selfbalancing device" and "other similar devices". However, ... Regulations 1986 and hence approval through European Community Whole Vehicle Type Approval. The government has been petitioned ... One can also use these devices on sidewalks at walking pace. Devices with a higher maximum speed are subject under the existing ... Legislative: Personal mobility device (Singapore Australia - Victoria Transport Policy Unit), Personal e-mobility device ( ...
*  Yellow trap
Interim Approval for Optional Use of Flashing Yellow Arrow for Permissive Left Turns (IA-10) from the Manual on Uniform Traffic ... despite clear prohibition from the Manual on Uniform Traffic Control Devices. (The Manual allows this only if a sign reading '" ...
*  Amber (color)
Uniform Provisions Concerning the Approval of Vehicles with Regard to the Installation of Lighting and Light-Signalling Devices ... 6: Uniform Provisions Concerning the Approval of Direction Indicators for Motor Vehicles and their Trailers (E/ECE/324-E/ECE/ ...
*  Selective yellow
Uniform Provisions Concerning the Approval of Vehicles with Regard to the Installation of Lighting and Light-Signalling Devices ... Uniform Provisions Concerning the Approval of Power-Driven Vehicle Front Fog Lamps SAE Standard J583: Front Fog Lamp ECE ... Japanese Industrial Standard JIS D-5500 Automobile Parts--Lighting and Light Signaling Devices p. 5, sec. 4.4.2, table #4 New ...
*  Research on Adverse Drug Events and Reports
Twenty-seven sADRs were associated with drugs and four were associated with a device. The success of the RADAR program has ... RADAR has analyzed historical data on many drugs from their initial inception, through approval by the FDA, and to the present ... Thus, the RADAR project has developed into an important adjunct to the current pharmaceutical drug and device safety system. ... Between 1998 and 2007, 33 serious adverse drug or device reactions have been reported by RADAR investigators. The toxicities ...
*  Williams FW15C
A press button starting device by means of which the clutch comes under automatic control, attracted the drivers unreserved ... approval during a succession of tests, but they did not use it in races, preferring the notional, psychological reassurance of ...
*  Medopad
... allows hospitals to pool their patient data into a single platform so it can be served to doctors' mobile devices in ... "Mobile health provider becomes first to receive CE approval". Retrieved 16 June 2014. "The Journal of mHealth". The Journal of ... Carl Reynolds, head of Open Health Care UK told New Scientist that an open system that worked on multiple devices would be ... In November 2013, Medopad became the first enterprise-class mobile health information system to receive CE approval. Some of ...
*  ISIRI 6484
ISIRI 6924, The type approval of motor vehicles and their trailers. Directive 92/6/EEC:1992 - on the installation and use of ... It defines "Speed limitation devices or similar speed limitation on-board systems of certain categories of motor vehicles". ... Directive 2004/11/EC of 11 February 2004 amending Council Directive 92/24/EEC relating to speed limitation devices or similar ... Other related sources are as follows: Directive 92/24/EEC of 31 March 1992 relating to speed limitation devices or similar ...
*  Preventice
Mayo device helps monitor heart patients from afar Medical Marketing & Media, May 22, 2013 Preventice announces commercial ... 2012 Home monitoring system for heart patients gets FDA approval The Post-Bulletin, September 11, 2012 Locally Made Remote ... 2013 Remote heart monitor device could improve ER triage, orthopedics surgical care (video) MedCity News, December 27, 2012 ... 2012 10 Wearable Health Tech Devices To Watch InformationWeek Healthcare, October 31, 2012 Healthcare Monitor Relies on ...
*  HAWK beacon
It was finally included in the 2009 edition of the US Manual on Uniform Traffic Control Devices as a "Pedestrian Hybrid Beacon ... United States transportation agencies wishing to use a HAWK signal were required to obtain approval from the Federal Highway ... A HAWK beacon (High-Intensity Activated crossWalK beacon) is a traffic control device used to stop road traffic and allow ... The Manual on Uniform Traffic Control Devices has guidelines that should be met before a HAWK beacon is installed. The ...
*  Los Angeles Chargers
The Chargers were given a one-year approval to relocate, conditioned on negotiating a lease agreement with the Rams or an ... through iOS and Android devices) as well as on their website. Most preseason games are televised on KABC-TV and KAZA-TV in Los ... The Chargers had continued preliminary work on a ballot initiative for public approval on a new facility. On November 8, 2016, ...
*  Imaging biomarker
For a pharmaceutical, device, or procedure to be approved for regular use in the U.S., it must be rigorously tested in clinical ... Section 112 of the Act gives explicit authority to give expedited approval for drugs that treat serious conditions as long as ... Although the act does not specifically mention the use of surrogate end-points for medical devices, section 205 requires that ... Other provisions enables monitoring of the products following market approval to ensure the efficacy of the surrogate end- ...