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

DIRECT HBA1C, FRUCTOSAMINE, GLUCOSE OXIDASE LIQUID

K Number: K080618 · Decision May 23, 2008
Classifications
1
FEI Numbers
65
Registration Numbers
65
Same Product Code
248
Applicant Total
20
Review Days
79

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Basic Information

Device Name
DIRECT HBA1C, FRUCTOSAMINE, GLUCOSE OXIDASE LIQUID
K Number
K080618
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7470
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Jas Diagnostics, Inc.
Date Received
March 5, 2008
Decision Date
May 23, 2008
Product Code
LCP
Advisory Committee
Hematology
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
LCP Assay, Glycosylated Hemoglobin

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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
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
K012038 JAS URIC ACID LIQUID REAGENT
Search all 20 clearances from Jas Diagnostics, Inc. →