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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.
This package includes following files:
| # | File Name | Document Date | Order ID: | Number of Pages | Price | |
|---|---|---|---|---|---|---|
| 1 |
R42130.pdf
|
Dec 28, 2011 | R42130 | 29 | $29.95 | Add to Cart |
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