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

RAICHEM GLUCOSE UV (LIQUID)

K Number: K041052 · Decision Jun 30, 2004
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
144
Applicant Total
52
Review Days
72

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Basic Information

Device Name
RAICHEM GLUCOSE UV (LIQUID)
K Number
K041052
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
April 19, 2004
Decision Date
June 30, 2004
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

Similar 510(k) Clearances

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

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Other Clearances by Hemagen Diagnostics, Inc.

K Number Device Name
K041051 RAICHEM BUN RATE REAGENT (LIQUID)
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
K012668 RAICHEM GLUCOSE UV REAGENT
Search all 52 clearances from Hemagen Diagnostics, Inc. →