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

KING DIAGNOSTIC TRIGLYCERIDES REAGENT

K Number: K922964 · Decision Aug 18, 1992
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
41
Review Days
60

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Basic Information

Device Name
KING DIAGNOSTIC TRIGLYCERIDES REAGENT
K Number
K922964
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
King Diagnostics, Inc.
Date Received
June 19, 1992
Decision Date
August 18, 1992
Product Code
CDT
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
CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CDT), ordered by most recent decision date.

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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)
K931326 KING DIAGNOSTICS CK REAGENT
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
Search all 41 clearances from King Diagnostics, Inc. →