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U.S. FDA approves Durata's acute bacterial skin infection drug

2014-05-24 01:29:08| Biotech - Topix.net

The U.S. Food and Drug Administration said on Friday it has approved a new drug to treat acute bacterial skin infections made by Durata Therapeutics Inc. Approval of the drug, Dalvance, follows a positive recommendation by the FDA's advisory committee, which also gave a favorable review to a rival product from Cubist Pharmaceuticals Inc. The FDA is ... (more)

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US: FDA approves aspartame-based sweetener Advantame

2014-05-20 13:02:00| Daily beverage news and comment - from just-drinks.com

An aspartame-based sweetener designed for use at low levels has won approval from the US Food and Drug Administration.

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FDA approves the Deka arm, the first commercial mind-controlled prosthetic arm

2014-05-12 15:45:11| Extremetech

The FDA has officially approved the first multi-input myoelectric artificial limb. The new Deka Arm System is designed to better replicate the full range of human function and was developed in conjunction with DARPA.

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FDA Approves ZONTIVITY (vorapaxar), First-in-Class PAR-1 Antagonist, for the Reduction of Thrombotic Cardiovascular Events in Patients with a History of Heart Attack or with Peripheral Arterial Disease

2014-05-12 13:30:00| Merck.com - Corporate News

Dateline City: WHITEHOUSE STATION, N.J. ZONTIVITY Added to Standard of Care Demonstrated Long-Term Benefit Through Three Years WHITEHOUSE STATION, N.J.--(BUSINESS WIRE)--Merck (NYSE:MRK), known as MSD outside the United States and Canada, today announced that the U.S. Food and Drug Administration (FDA) has approved ZONTIVITY (vorapaxar) for the reduction of thrombotic cardiovascular events in patients with a history of heart attack (myocardial infarction) or in patients with narrowing of leg arteries, called peripheral arterial disease (PAD). Language: English Contact: MerckMedia:Pamela Eisele, 267-305-3558orPatrick Witmer, 267-305-4910orInvestors:Carol Ferguson, 908-423-4465orJustin Holko, 908-423-5088 Ticker Slug: Ticker: MRK Exchange: NYSE read more

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FDA Approves Segway Inventor's Mind-Controlled Robotic Arm

2014-05-12 04:59:47| Automakers - Topix.net

The era of real cyborgs has begun. The U.S. Food and Drug Administration gave its first approval for the sale and marketing of a prosthetic arm that translates signals from a person's muscles on Friday.

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