FDA PMA FDA Class 3 Approved 🇺🇸 United States

Permanent Pacemaker Electrode

PMA: P830061 · Supplement: S003 · Decision Jun 30, 1987
Classifications
1
FEI Numbers
24
Registration Numbers
24

Basic Information

Device Name
Permanent Pacemaker Electrode
Trade Name
MEDTRONIC{R} CAP SURE{TM} MODEL 4003/4503 PACING
PMA Number
P830061
Supplement Number
S003
Device Class
FDA Class 3
Product Code
DTB
Generic Name
permanent pacemaker Electrode
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
June 30, 1987
Date Received
February 2, 1987
Supplement Type
Normal 180 Day Track
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DTB Permanent Pacemaker Electrode