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

FINGER PAINGUARD CAT.#193-194

K Number: K802015 · Decision Sep 9, 1980
Classifications
1
FEI Numbers
681
Registration Numbers
681
Same Product Code
41
Applicant Total
31
Review Days
20

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Basic Information

Device Name
FINGER PAINGUARD CAT.#193-194
K Number
K802015
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5075
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Pollak (Intl.), Ltd.
Date Received
August 20, 1980
Decision Date
September 9, 1980
Product Code
FQM
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FQM Bandage, Elastic

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Other Clearances by Pollak (Intl.), Ltd.

K Number Device Name
K000227 UMBICUT
K810049 PEDICAT*
K810050 VECAFIX*
K802009 FLOWCLAMP CAT.#1011 & 1012
K802011 INFUSSION ALARM SYSTEM I.A.S. CAT.#1118
K802017 DRESSING CHANGE SET CAT.#910-930
K802007 PEDIWET=GUAZE IMPREGNATED WITH PETROL
K801991 PLASTIC FORCEPS CAT.#1001-1010
K801996 GUAZE BANDAGES CAT.#101-169
K802021 PEDIBAND CAT.#195-197
Search all 31 clearances from Pollak (Intl.), Ltd. →