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

KING DIAGNOSTICS CK REAGENT

K Number: K931326 · Decision Jun 15, 1993
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
122
Applicant Total
41
Review Days
91

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Basic Information

Device Name
KING DIAGNOSTICS CK REAGENT
K Number
K931326
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1215
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
King Diagnostics, Inc.
Date Received
March 16, 1993
Decision Date
June 15, 1993
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 King Diagnostics, Inc.

K Number Device Name
K933329 KING DIAGNOSTICS IRON AND TOTAL IRON BINDING CAPACITY REAGENT
K931834 KING SODIUM/POTASSIUM STANDARD MODIFIED
K931773 HDL PRECIPITATING REAGENT (DEXTRAN SULFATE)
K923129 KING DIAGNOSTICS GLUCOSE (HK) REAGENT
K922969 KING DIAGNOSTICS UREA NITROGEN REAGENT
K922921 KING DIAGNOSTICS CHLORIDE REAGENT
K923927 KING DIAGNOSTICS MAGNESIUM REAGENT
K923091 KING DIAGNOSTICS GAMMA GT REAGENT
K923128 KING DIAGNOSTICS CHOLESTEROL REAGENT
K922964 KING DIAGNOSTIC TRIGLYCERIDES REAGENT
Search all 41 clearances from King Diagnostics, Inc. →