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

FDA-INTENT-TO-EXEMPT - 7/2015 EDITION - SUPERSEDED
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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


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Document Number

FDA-INTENT-TO-EXEMPT

Revision Level

7/2015 EDITION

Status

Superseded

Publication Date

July 1, 2015

Page Count

14 pages