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

IGA ANTI-GLIADIN (IGA-AGA) ANTIBODY TEST KIT

K Number: K964341 · Decision May 30, 1997
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
41
Applicant Total
55
Review Days
211

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Basic Information

Device Name
IGA ANTI-GLIADIN (IGA-AGA) ANTIBODY TEST KIT
K Number
K964341
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5750
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Immco Diagnostics, Inc.
Date Received
October 31, 1996
Decision Date
May 30, 1997
Product Code
MST
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
MST Antibodies, Gliadin

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K163177 ImmuLisa Enhanced Gliadin IgA Antibody ELISA, ImmuLisa Enhanced Gliadin IgG Antibody ELISA
K162788 ImmuLisa Enhanced B2GP1 IgA Antibody ELISA, ImmuLisa Enhanced B2GP1 IgG Antibody ELISA, ImmuLisa Enhanced B2GP1 IgM Antibody ELISA, ImmuLisa Enhanced B2GP1 IgA/IgG/IgM Antibody ELISA
K151559 ImmuLisa Enhanced Centromere Antibody ELISA
K143736 ImmuLisa Enhanced RF IgA Antibody ELISA, ImmuLisa Enhanced RF IgG Antibody ELISA, ImmuLisa Enhanced RF IgM Antibody ELISA, ImmuLisa Enhanced RF Antibody Screen ELISA
K142781 ImmuLisa Enhanced SS-A (Ro) Antibody ELISA, ImmuLisa Enhanced SS-B (La) Antibody ELISA, ImmuLisa Enhanced Sm Antibody ELISA, ImmuLisa Enhanced RNP Antibody ELISA
K123713 IMMULISA ENHANCED CELIAC FUSION (TTG/DGP) IGA/IGG ANTIBODY ELISA
K113020 IMMULISA ENHANCED (TM) CARDIOLIPIN IGA, IGG, IGM AND IGA/IGG/IGM ANTIBODY (ACA) ELISAS
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