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

    LA-HISTO ANTIBODY SYSTEM #HL 1001

    K Number: K830837 · Decision May 5, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    2
    Registration Numbers
    2
    Same Product Code
    11
    Applicant Total
    26
    Review Days
    50

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    Basic Information

    Device Name
    LA-HISTO ANTIBODY SYSTEM #HL 1001
    K Number
    K830837
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.3320
    Medical Specialty
    Microbiology
    Decision
    Substantially Equivalent
    Applicant
    Immuno-Mycologics, Inc.
    Date Received
    March 16, 1983
    Decision Date
    May 5, 1983
    Product Code
    GMJ
    Advisory Committee
    Microbiology
    Review Advisory Committee
    MI
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GMJ Antigens, Histoplasma Capsulatum, All

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    Other Clearances by Immuno-Mycologics, Inc.

    K Number Device Name
    K120946 ALPHA CRYPTOCOCCAL ANTIGEN EIA
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    K102286 CRAG LATERAL FLOW ASSAY (CRAG LFA)
    K101407 ALPHA HISTOPLASMA ANTIGEN EIA MODEL HAG102
    K883333 RABBIT PLASMA FIBRINOGEN (RPF) SUPPLEMENT
    K880029 EXO-ANTIGEN IDENTIFICATION SYSTEM CAT.# EX1001
    K843286 EI-CANDIDA ENZYME IMMUNOASSAY EI1001
    K831918 LA-STAPH IDENTIFICATION SYSTEM
    K810510 YA-CRYPTO ANTIBODY TUBE AGGLUTINATION
    K802427 LA-SPORO ANTIBODY SYSTEM
    Search all 26 clearances from Immuno-Mycologics, Inc. →