FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

ELECTRODE, TEMPORARY MYOCARDIAL

K Number: K760513 · Decision Oct 15, 1976
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
11
Review Days
51

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Basic Information

Device Name
ELECTRODE, TEMPORARY MYOCARDIAL
K Number
K760513
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Winn Hirsch & Assoc.
Date Received
August 25, 1976
Decision Date
October 15, 1976
Product Code
DTB
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DTB Permanent Pacemaker Electrode

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Other Clearances by Winn Hirsch & Assoc.

K Number Device Name
K880309 TYPE 316L STAINLESS STEEL WIRE
K864375 TYPE 316L COTTER WIRE
K832213 GAUZE CONVERSION CLASS II STERILE
K832214 GAUZE CONVERSION CLASS I-NON-STERILE
K830511 ZANLEX, ZAN-TEX & ZANDEX
K812391 NEUROSPONGES
K812390 NEUROSPONGE PADDIE
K800195 COTTON UNDER CAST PADDING
K761155 CELLULOSE EYE STICK
K760365 BLANKET, BURN
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