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

IMMULISA MPO ANTIBODY ELISA

K Number: K092599 · Decision Oct 7, 2010
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
73
Applicant Total
55
Review Days
409

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Basic Information

Device Name
IMMULISA MPO ANTIBODY ELISA
K Number
K092599
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5660
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Immco Diagnostics, Inc.
Date Received
August 24, 2009
Decision Date
October 7, 2010
Product Code
MOB
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
MOB Test System, Antineutrophil Cytoplasmic Antibodies (Anca)

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Other Clearances by Immco Diagnostics, Inc.

K Number Device Name
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K163133 ImmuLisa Enhanced AMA IgG Antibody ELISA; ImmuLisa Enhanced AMA IgA/IgG/IgM Antibody ELISA
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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