FDA-INTENT-TO-EXEMPT › 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-2019.pdf
Revision Level
2019 EDITION
Status
Current
Publication Date
Feb. 8, 2019
Page Count
6 pages