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

VECAFIX*

K Number: K810050 · Decision Mar 26, 1981
Classifications
1
FEI Numbers
972
Registration Numbers
972
Same Product Code
186
Applicant Total
31
Review Days
72

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Basic Information

Device Name
VECAFIX*
K Number
K810050
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5240
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Pollak (Intl.), Ltd.
Date Received
January 13, 1981
Decision Date
March 26, 1981
Product Code
KGX
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
KGX Tape And Bandage, Adhesive

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Other Clearances by Pollak (Intl.), Ltd.

K Number Device Name
K000227 UMBICUT
K810049 PEDICAT*
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
K802022 STERILE GUAZE SWABS CAT.#301-420
Search all 31 clearances from Pollak (Intl.), Ltd. →