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

QUANTAFFIRM CPK ISO ENZYME SERUM (HUMAN)

K Number: K791723 · Decision Oct 1, 1979
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
96
Applicant Total
41
Review Days
32

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Basic Information

Device Name
QUANTAFFIRM CPK ISO ENZYME SERUM (HUMAN)
K Number
K791723
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Organon, Inc.
Date Received
August 30, 1979
Decision Date
October 1, 1979
Product Code
JJT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
JJT Enzyme Controls (Assayed And Unassayed)

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Other Clearances by Organon, Inc.

K Number Device Name
K950861 RECONSTITUTION ACCESSOREIS
K853388 MONOSTICON UNI-DOT
K842314 DUOCLON COLOR-CEPT
K841525 OREIA II B-HCG PREGNANCY TEST KIT
K841602 ACCURATE BETA 30 PREGNANCY TEST KIT
K840650 B-NEOCEPT 30
K832801 OREIA II B-HCG, ENZYME INNUNOASSAY
K831339 NEO-PREGNOSTICON DUOCLON TUBE TEST
K831109 DUOCLON SLIDE TEST
K823682 BETA FFIRM TEST
Search all 41 clearances from Organon, Inc. →