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

TRIGLYCERIDE REAGENT (UV)

K Number: K823709 · Decision Jan 7, 1983
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
50
Review Days
29

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Basic Information

Device Name
TRIGLYCERIDE REAGENT (UV)
K Number
K823709
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Gilford Diagnostics
Date Received
December 9, 1982
Decision Date
January 7, 1983
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

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Other Clearances by Gilford Diagnostics

K Number Device Name
K832094 BILIRUBIN CALIBRATORS & CONTROL
K831844 DIRECT BILIRUBIN REAGENT
K831843 GILCHEM TOTAL BILIRUBIN REAGENT
K822739 AHBD
K822334 BILIRUBIN CALIBRATORS
K822289 CO2/CI STANDARDS
K822149 GILCHEM Y-GT REAGENT
K821719 AMMONIA REAGENT
K820976 GIL CHEM MAGNESIUM REAGENT
K820975 GILCHEM ACID PHOSPHATASE REAGENT
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