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

    MODELS TA 1017 & 1017T GRITIFLO DISPOS

    K Number: K811538 · Decision Jun 12, 1981
    View on FDA
    Classifications
    1
    FEI Numbers
    87
    Registration Numbers
    87
    Same Product Code
    147
    Applicant Total
    31
    Review Days
    11

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    Basic Information

    Device Name
    MODELS TA 1017 & 1017T GRITIFLO DISPOS
    K Number
    K811538
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2850
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Gould, Inc.
    Date Received
    June 1, 1981
    Decision Date
    June 12, 1981
    Product Code
    DRS
    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
    DRS Transducer, Blood-Pressure, Extravascular

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