FDA-EVALUATING › The 510(k) Program: Evaluating Substantial Equivalence in Premarket Notifications [510(k)] - Guidance for Industry and Food and Drug Administration Staff
The 510(k) Program: Evaluating Substantial Equivalence in Premarket Notifications [510(k)] - Guidance for Industry and Food and Drug Administration Staff
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Document Number
FDA-EVALUATING
Revision Level
2014 EDITION
Status
Current
Publication Date
July 28, 2014
Page Count
42 pages