FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BLANKET, BURN

K Number: K760365 · Decision Aug 11, 1976
Classifications
1
FEI Numbers
58
Registration Numbers
58
Same Product Code
16
Applicant Total
11
Review Days
8

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Basic Information

Device Name
BLANKET, BURN
K Number
K760365
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5180
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Winn Hirsch & Assoc.
Date Received
August 3, 1976
Decision Date
August 11, 1976
Product Code
FPY
Advisory Committee
General Hospital
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
FPY Sheet, Burn

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K880309 TYPE 316L STAINLESS STEEL WIRE
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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
K760513 ELECTRODE, TEMPORARY MYOCARDIAL
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