FDA Regulation of Medical Devices

This report provides a description of FDA's medical device review process divided into two parts: premarket requirements and postmarket requirements. Appendix A provides a history of laws governing medical device regulation and Appendix B provides a table of acronyms used in the report. Bills: H.R. 5651, S. 3187


This package includes following files:

#	File Name	Document Date	Order ID:	Number of Pages	Price
1	R42130.pdf	Jun 25, 2012	R42130	29	$29.95	Add to Cart

Older Versions:

FDA Regulation of Medical Devices  [Order No: R42130  Release Date: May 18,2012  Pages: 29]

FDA Regulation of Medical Devices  [Order No: R42130  Release Date: Dec 28,2011  Pages: 29]