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

    STANICOR, OMNI-STAN,MOD 333B,334A GAMMA

    K Number: K792348 · Decision Dec 5, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    3
    Same Product Code
    9
    Applicant Total
    315
    Review Days
    16

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    Basic Information

    Device Name
    STANICOR, OMNI-STAN,MOD 333B,334A GAMMA
    K Number
    K792348
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4300
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Cordis Corp.
    Date Received
    November 19, 1979
    Decision Date
    December 5, 1979
    Product Code
    DTX
    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
    DTX Gas Control Unit, Cardiopulmonary Bypass

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