FDA-INTENT-TO-EXEMPT › Historical Revision Information
Intent to Exempt Certain Unclassified, Class II, and Class I Reserved Medical Devices from Premarket Notification Requirements - Guidance for Industry and Food and Drug Administration Staff
Intent to Exempt Certain Unclassified, Class II, and Class I Reserved Medical Devices from Premarket Notification Requirements - Guidance for Industry and Food and Drug Administration Staff
This document comes with our free Notification Service, good for the life of the document.
This document is available in either Paper or PDF format.
Document Number
FDA-INTENT-TO-EXEMPT
Revision Level
8/2015 EDITION
Status
Superseded
Publication Date
Aug. 14, 2015
Page Count
14 pages