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

HORIZON DIAGNOSTICS TRIGLYCERIDES-GPO REAGENT

K Number: K933722 · Decision Jun 13, 1996
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
7
Review Days
1046

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Basic Information

Device Name
HORIZON DIAGNOSTICS TRIGLYCERIDES-GPO REAGENT
K Number
K933722
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Horizon Diagnostics, Inc.
Date Received
August 2, 1993
Decision Date
June 13, 1996
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 Horizon Diagnostics, Inc.

K Number Device Name
K971566 CREATINE KINASE-MB REAGENT SET
K935712 IRON/TIBC REAGENT
K930678 AMYLASE
K934533 BUN-300/BUN-500 UREA NITROGEN REAGENT
K930679 DIRECT BILIRUBIN
K930074 IN-VITRO DIAGNOSTIC REAGENT SET