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

HEMAGEN ENA [JO-I] KIT

K Number: K902139 · Decision May 18, 1990
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
109
Applicant Total
52
Review Days
9

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Basic Information

Device Name
HEMAGEN ENA [JO-I] KIT
K Number
K902139
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Hemagen Diagnostics, Inc.
Date Received
May 9, 1990
Decision Date
May 18, 1990
Product Code
DHN
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

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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
Search all 52 clearances from Hemagen Diagnostics, Inc. →