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

MODIFICATION TO RAICHEM CALCIUM REAGENT

K Number: K022049 · Decision Jul 19, 2002
Classifications
1
FEI Numbers
29
Registration Numbers
29
Same Product Code
46
Applicant Total
52
Review Days
25

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Basic Information

Device Name
MODIFICATION TO RAICHEM CALCIUM REAGENT
K Number
K022049
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
862.1145
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hemagen Diagnostics, Inc.
Date Received
June 24, 2002
Decision Date
July 19, 2002
Product Code
CJY
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
CJY Azo Dye, Calcium

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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
K021194 RAICHEM CRP HIGH SENSITIVITY TEST SYSTEM
K012649 RAICHEM BUN RATE REAGENT
K012668 RAICHEM GLUCOSE UV REAGENT
Search all 52 clearances from Hemagen Diagnostics, Inc. →