BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇩🇪 Germany

    BETASTAR 1131.02 MOBILE OPERATING TABLE

    K Number: K926525 · Decision Oct 12, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    73
    Registration Numbers
    73
    Same Product Code
    34
    Applicant Total
    10
    Review Days
    286

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    Basic Information

    Device Name
    BETASTAR 1131.02 MOBILE OPERATING TABLE
    K Number
    K926525
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4960
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Stierlen-Maquet AG
    Date Received
    December 30, 1992
    Decision Date
    October 12, 1993
    Product Code
    FQO
    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
    FQO Table, Operating-Room, Ac-Powered

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