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

CREATININE

K Number: K003247 · Decision Dec 14, 2000
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
158
Applicant Total
20
Review Days
58

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Basic Information

Device Name
CREATININE
K Number
K003247
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1225
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Jas Diagnostics, Inc.
Date Received
October 17, 2000
Decision Date
December 14, 2000
Product Code
CGX
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
CGX Alkaline Picrate, Colorimetry, Creatinine

Similar 510(k) Clearances

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

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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)
K013698 AST (SGOT)
K012332 JAS CARBON DIOXIDE LIQUID REAGENT
Search all 20 clearances from Jas Diagnostics, Inc. →