Medical Device Databases | FDA
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Manufacturers required to conduct PAS must complete the study as a condition of approval. This database allows you to search PAS ... Skiptomaincontent SkiptoFDASearch Skiptointhissectionmenu Skiptofooterlinks Inthissection: DeviceAdvice:Comprehen
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- 1Medical Device Databases | FDA
Manufacturers required to conduct PAS must complete the study as a condition of approval. This da...
- 2Premarket Approval (PMA) - US Food and Drug Administration
Premarket approval (PMA) is the FDA process of scientific and regulatory review to evaluate the s...
- 3Device Approvals, Denials and Clearances | FDA
510(k) (premarket notification) to FDA is required at least 90 days before marketing unless the d...
- 4510(k) Database - 510(k) Premarket Notification
A 510(K) is a premarket submission made to FDA to demonstrate that the device to be marketed is a...
- 5Search Databases | FDA
Animal Drugs @ FDA is an online database of FDA-approved animal drugs. It is searchable by NADA/A...
