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

IN-VITRO TEST DETERMINATION OF TRIALYCERIDE

K Number: K854182 · Decision Nov 25, 1985
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
36
Review Days
41

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Basic Information

Device Name
IN-VITRO TEST DETERMINATION OF TRIALYCERIDE
K Number
K854182
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Clinical Data, Inc.
Date Received
October 15, 1985
Decision Date
November 25, 1985
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

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Other Clearances by Clinical Data, Inc.

K Number Device Name
K071706 ENVOY 500 HDL; CHOLESTEROL REAGENT KIT (MODEL# 55301), CALIBRATOR KIT (MODEL# 55118)
K052591 NANOPIA WIDE RANGE C-REACTIVE PROTEIN (CRP) REAGENT KIT
K033983 VITALAB IRON REAGENT
K040631 VITALAB DIRECT BILIRUBIN REAGENT
K040534 VITALAB AMYLASE REAGENT
K034000 VITALAB TRIGLYCERIDES REAGENT AND VITALAB CALIBRATOR
K040508 VITALAB MAGNESIUM REAGENT
K040467 VITALAB URIC ACID REAGENT
K031042 ATAC HEMOGLOBIN A1C REAGENT KIT
K031044 ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR
Search all 36 clearances from Clinical Data, Inc. →