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

HEMAGEN ENA SCREEN-6 KIT (EIA METHOD)

K Number: K935828 · Decision Apr 20, 1994
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
179
Applicant Total
52
Review Days
134

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Basic Information

Device Name
HEMAGEN ENA SCREEN-6 KIT (EIA METHOD)
K Number
K935828
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hemagen Diagnostics, Inc.
Date Received
December 7, 1993
Decision Date
April 20, 1994
Product Code
LLL
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
LLL Extractable Antinuclear Antibody, Antigen And Control

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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
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