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

FLOWCLAMP CAT.#1011 & 1012

K Number: K802009 · Decision Oct 31, 1980
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
5
Applicant Total
31
Review Days
72

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Basic Information

Device Name
FLOWCLAMP CAT.#1011 & 1012
K Number
K802009
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
876.4730
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Pollak (Intl.), Ltd.
Date Received
August 20, 1980
Decision Date
October 31, 1980
Product Code
FKK
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
FKK Clamp, Line

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Other Clearances by Pollak (Intl.), Ltd.

K Number Device Name
K000227 UMBICUT
K810049 PEDICAT*
K810050 VECAFIX*
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. →