FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CENTRIFICHEM CK

K Number: K800127 · Decision Feb 13, 1980
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
122
Applicant Total
69
Review Days
26

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Basic Information

Device Name
CENTRIFICHEM CK
K Number
K800127
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Union Carbide Corp.
Date Received
January 18, 1980
Decision Date
February 13, 1980
Product Code
CGS
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
CGS Nad Reduction/Nadh Oxidation, Cpk Or Isoenzymes

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Other Clearances by Union Carbide Corp.

K Number Device Name
K830337 MARK III OXYGEN WALKER SYS-LOW PRESS
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K820535 LASER GAS MIXTURES
K812536 LINDE MARK II
K810732 LINDE MARK II OXYGEN RESERV. TYPE OR-4
K810596 CENTRIFI CHEM SYSTEM 400 ANALYZER
K810129 CENTRIFICHEM SYSTEM 500
K803216 CENTRIFICHEM AST/SGOT OPTIMIZED REAGENT
K802741 CENTRIFICHEM COMB. SERUM-BASED CALIB.
K802520 CENTRIFICHEM PIPETTOR ACCURACY CALIB.
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