BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    THE VERSA-BED

    K Number: K792298 · Decision Dec 20, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    221
    Registration Numbers
    221
    Same Product Code
    38
    Applicant Total
    1
    Review Days
    37

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    Basic Information

    Device Name
    THE VERSA-BED
    K Number
    K792298
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.5120
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    First & Ten, Inc.
    Date Received
    November 13, 1979
    Decision Date
    December 20, 1979
    Product Code
    FNJ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FNJ Bed, Manual

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