BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇬🇷 Greece

    OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.

    K Number: K883613 · Decision Sep 15, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    111
    Registration Numbers
    111
    Same Product Code
    17
    Applicant Total
    10
    Review Days
    24

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    Basic Information

    Device Name
    OPER. TABLE FOR PERCUTAN. TRANS. CORONARY ANGIO.
    K Number
    K883613
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4960
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Stierlen-Maquet AG
    Date Received
    August 22, 1988
    Decision Date
    September 15, 1988
    Product Code
    GDC
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    GDC Table, Operating-Room, Electrical

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