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

    OPERATING TABLE SYSTEM-BETAMAQUET 1140

    K Number: K920890 · Decision Jul 2, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    73
    Registration Numbers
    73
    Same Product Code
    34
    Applicant Total
    10
    Review Days
    141

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    Basic Information

    Device Name
    OPERATING TABLE SYSTEM-BETAMAQUET 1140
    K Number
    K920890
    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
    February 12, 1992
    Decision Date
    July 2, 1992
    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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