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) (CPG 7124.30) REVOKED

Compliance Policy Guide

Compliance Policy Guidance for FDA Staff

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) (CPG 7124.30)

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)