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

NEUROSPONGES

K Number: K812391 · Decision Nov 24, 1981
Classifications
1
FEI Numbers
211
Registration Numbers
211
Same Product Code
110
Applicant Total
11
Review Days
96

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Basic Information

Device Name
NEUROSPONGES
K Number
K812391
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4450
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Winn Hirsch & Assoc.
Date Received
August 20, 1981
Decision Date
November 24, 1981
Product Code
GDY
Advisory Committee
General, Plastic Surgery
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
GDY Gauze/Sponge, Internal, X-Ray Detectable

Similar 510(k) Clearances

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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
K812390 NEUROSPONGE PADDIE
K800195 COTTON UNDER CAST PADDING
K761155 CELLULOSE EYE STICK
K760513 ELECTRODE, TEMPORARY MYOCARDIAL
K760365 BLANKET, BURN
Search all 11 clearances from Winn Hirsch & Assoc. →