FDA-INTENT-TO-EXEMPT Complete Document History
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

Complete Current Edition:
   2019 EDITION - Guidance for Industry and Food and Drug Administration Staff - Feb. 8, 2019

Obsolete Revision Information:
   8/2015 EDITION - Guidance for Industry and Food and Drug Administration Staff - Aug. 14, 2015
   7/2015 EDITION - Guidance for Industry and Food and Drug Administration Staff - July 1, 2015
   2014 DRAFT - Draft Guidance for Industry and Food and Drug Administration - Aug. 1, 2014