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

    RADIAL IMMUNODIFFUSION KIT-IMMUNOGLOB.

    K Number: K772076 · Decision Feb 3, 1978
    View on FDA
    Classifications
    1
    FEI Numbers
    21
    Registration Numbers
    21
    Same Product Code
    53
    Applicant Total
    11
    Review Days
    92

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    Basic Information

    Device Name
    RADIAL IMMUNODIFFUSION KIT-IMMUNOGLOB.
    K Number
    K772076
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    866.5510
    Medical Specialty
    Immunology
    Decision
    Substantially Equivalent
    Applicant
    Gelman Instrument Co.
    Date Received
    November 3, 1977
    Decision Date
    February 3, 1978
    Product Code
    CZP
    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
    CZP Iga, Antigen, Antiserum, Control

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    Other Clearances by Gelman Instrument Co.

    K Number Device Name
    K772075 RADIAL IMMUNODIFFUSION KIT-COMPLEMENT
    K772080 RADIAL IMMUNODIFFUSION KIT-ALPH-L-ANTIT
    K772077 RADIAL IMMUNODIFFUSION KIT-IMMUNOGLOB.G
    K772074 RADIAL IMMUNODIFFUSION KIT-TRANSFERRIN
    K772079 RADIAL IMMUNODIFFUSION KIT-IMMUNOGLOB.M
    K772073 RADIAL IMMUNODIFFUSION KIT-COMP. 3
    K772078 RADIAL IMMUNODIFFUSION KIT-HAPTOGLOBIN
    K772325 DENSITOMETER 18, COMPUTING, AUTO.
    K771812 LIPPOPROTEIN ELECTROPHORESIS REAGENT SET
    K770155 ALKALINE PHOSPHATASE ISOYZME REAGENT SET
    Search all 11 clearances from Gelman Instrument Co. →