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

    AQUAMATIC K-MODULE MODEL K-20

    K Number: K771537 · Decision Sep 6, 1977
    View on FDA
    Classifications
    1
    FEI Numbers
    90
    Registration Numbers
    90
    Same Product Code
    157
    Applicant Total
    6
    Review Days
    26

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    Basic Information

    Device Name
    AQUAMATIC K-MODULE MODEL K-20
    K Number
    K771537
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.5900
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Gorman Rupp Industries
    Date Received
    August 11, 1977
    Decision Date
    September 6, 1977
    Product Code
    DWJ
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DWJ System, Thermal Regulating

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    K760910 DISPOSABLE K-PADS
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