FDA-EVALUATING The 510(k) Program: Evaluating Substantial Equivalence in Premarket Notifications [510(k)] - Guidance for Industry and Food and Drug Administration Staff

FDA-EVALUATING - 2014 EDITION - CURRENT
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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