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

AST (SGOT)

K Number: K013698 · Decision Dec 21, 2001
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
138
Applicant Total
20
Review Days
44

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Basic Information

Device Name
AST (SGOT)
K Number
K013698
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1100
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Jas Diagnostics, Inc.
Date Received
November 7, 2001
Decision Date
December 21, 2001
Product Code
CIT
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
CIT Nadh Oxidation/Nad Reduction, Ast/Sgot

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Other Clearances by Jas Diagnostics, Inc.

K Number Device Name
K130915 XL-200 CLINICAL CHEMISTRY ANALYZER, JAS GLUCOSE REAGENT, ISE REAGENT PACK
K080623 CHOLESTEROL OXIDASE JASE, AND GLYCEROL INASE TRIGLYCERIDES, MODEL NA
K080618 DIRECT HBA1C, FRUCTOSAMINE, GLUCOSE OXIDASE LIQUID
K022519 LDL CHOLESTEROL (AUTOMATED)
K021671 JAS HDL CHOLESTEROL (AUTOMATED) REAGENT
K020454 CHEMISTRY CALIBRATOR
K020282 JAS AMYLASE LIQUID REAGENT
K013912 CREATINE KINASE (CK-NAC)
K012332 JAS CARBON DIOXIDE LIQUID REAGENT
K012038 JAS URIC ACID LIQUID REAGENT
Search all 20 clearances from Jas Diagnostics, Inc. →