FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

RAICHEM LDL-CHOLESTEROL DIRECT REAGENT

K Number: K022772 · Decision Sep 17, 2002
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
30
Applicant Total
52
Review Days
27

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Basic Information

Device Name
RAICHEM LDL-CHOLESTEROL DIRECT REAGENT
K Number
K022772
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hemagen Diagnostics, Inc.
Date Received
August 21, 2002
Decision Date
September 17, 2002
Product Code
MRR
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
MRR System, Test, Low Density, Lipoprotein

Similar 510(k) Clearances

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Other Clearances by Hemagen Diagnostics, Inc.

K Number Device Name
K041052 RAICHEM GLUCOSE UV (LIQUID)
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
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. →