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

SIGMA PROCEDURE 47-UV

K Number: K842013 · Decision Jun 25, 1984
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
122
Applicant Total
231
Review Days
39

Basic Information

Device Name
SIGMA PROCEDURE 47-UV
K Number
K842013
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
SIGMA CHEMICAL CO.
Date Received
May 17, 1984
Decision Date
June 25, 1984
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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K Number Device Name
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K933679 SIGMA BUN REAGENT
K933691 SIGMA CO2 ALKALINE BUFFER REAGENT
K933703 SIGMA WASH CONCENTRATE SOLUTION
K933692 SIGMA CO2 ACID REAGENT
K933695 SIGMA ELECTROLYTE BUFFER
K933697 SIGMA CRE REAGENT
K933693 SIGMA CX-3 CALIBRATION STANDARD LEVEL 2
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