Inspections, Compliance, Enforcement, and Criminal Investigations

CPG Sec. 300.700 Direct Reference Authority for Class III Medical Devices Without a Premarket Notification (510(k)) or an Approved Premarket Approval Application (PMA) REVOKED

Revocation/Deletion

Sec. 300.700 Direct Reference Authority for Class III Medical Devices Without a Premarket Notification (510(k)) or an Approved Premarket Approval Application (PMA)

REVOKED effective October 07, 2002 per Federal Register dated September 05, 2002 (67 FR 56850)

Issued: 2/26/91
Revised: 3/95
REVOKED: 10/07/2002 (Federal Register 09/05/2002)


Page created 10/15/2002 (tc)

Page Last Updated: 03/20/2015
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