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

CK(OPTIMIZED) REAGENT

K Number: K854501 · Decision Dec 4, 1985
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
122
Applicant Total
164
Review Days
22

Basic Information

Device Name
CK(OPTIMIZED) REAGENT
K Number
K854501
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
SIGMA DIAGNOSTICS, INC.
Date Received
November 12, 1985
Decision Date
December 4, 1985
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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K013545 SIGMA DIAGNOSTICS AUTO D-DIMER CONTROL, LEVEL 3, MODEL A8221
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K010158 THROMBOMAX-HS WITH CALCIUM, MODEL T6540
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