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

RAICHEM GLUCOSE UV REAGENT

K Number: K012668 · Decision Oct 15, 2001
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
142
Applicant Total
52
Review Days
63

Basic Information

Device Name
RAICHEM GLUCOSE UV REAGENT
K Number
K012668
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1345
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
HEMAGEN DIAGNOSTICS, INC.
Date Received
August 13, 2001
Decision Date
October 15, 2001
Product Code
CFR
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
CFR Hexokinase, Glucose

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Other Clearances by HEMAGEN DIAGNOSTICS, INC.

K Number Device Name
K041052 RAICHEM GLUCOSE UV (LIQUID)
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K041009 RAICHEM CALCIUM (OCPC) LIQUID REAGENT
K031101 RAICHEM ASSAYED CONTROL SERUM LEVEL 1 & 2
K023784 RAICHEM HDL CHOLESTEROL USING CANTROL HDL PRECIPITATING TUBES ON THE COBAS MIRA ANAYLZER
K022772 RAICHEM LDL-CHOLESTEROL DIRECT REAGENT
K022767 RAICHEM LIPID CALIBRATOR
K021194 RAICHEM CRP HIGH SENSITIVITY TEST SYSTEM
K022049 MODIFICATION TO RAICHEM CALCIUM REAGENT
K012649 RAICHEM BUN RATE REAGENT
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