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

EYE PADS CAT.#581-599

K Number: K801995 · Decision Sep 9, 1980
Classifications
1
FEI Numbers
172
Registration Numbers
172
Same Product Code
16
Applicant Total
31
Review Days
20

Basic Information

Device Name
EYE PADS CAT.#581-599
K Number
K801995
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4440
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Pollak (Intl.), Ltd.
Date Received
August 20, 1980
Decision Date
September 9, 1980
Product Code
HMP
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
HMP Pad, Eye

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K Number Device Name
K000227 UMBICUT
K810049 PEDICAT*
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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
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