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U.S. Department of Health and Human Services

Inspections, Compliance, Enforcement, and Criminal Investigations

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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)

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