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

RAICHEM CRP HIGH SENSITIVITY TEST SYSTEM

K Number: K021194 · Decision Jul 29, 2002
Classifications
1
FEI Numbers
46
Registration Numbers
46
Same Product Code
125
Applicant Total
52
Review Days
105

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Basic Information

Device Name
RAICHEM CRP HIGH SENSITIVITY TEST SYSTEM
K Number
K021194
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5270
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hemagen Diagnostics, Inc.
Date Received
April 15, 2002
Decision Date
July 29, 2002
Product Code
DCK
Advisory Committee
Immunology
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
DCK C-Reactive Protein, Antigen, Antiserum, And Control

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
K022772 RAICHEM LDL-CHOLESTEROL DIRECT REAGENT
K022767 RAICHEM LIPID CALIBRATOR
K022049 MODIFICATION TO RAICHEM CALCIUM REAGENT
K012649 RAICHEM BUN RATE REAGENT
K012668 RAICHEM GLUCOSE UV REAGENT
Search all 52 clearances from Hemagen Diagnostics, Inc. →