510(k) K883602

BIOPORE VS.1 ENDOCARDIAL INTER IMPLANT PACING LEAD by Intermedics, Inc. — Product Code DTB

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 6, 1988
Date Received
August 23, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Permanent Pacemaker Electrode
Device Class
Class III
Regulation Number
870.3680
Review Panel
CV
Submission Type