Medical Devices: FDA's Premarket Review and Postmarket Safety Efforts: Gao-11-556t

The Food and Drug Administration (FDA) is responsible for overseeing medical devices sold in the United States. In general, new devices are subject to FDA review via either the 510(k) premarket... This description may be from another edition of this product.

• Format: Paperback
• Language: English
• ISBN: 1287209262
• ISBN13: 9781287209263
• Release Date: May 2013
• Publisher: Bibliogov
• Length: 26 Pages
• Weight: 0.15 lbs.
• Dimensions: 0.1" x 7.4" x 9.7"