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

    DITTMAR POWER LIFTER

    K Number: K883260 · Decision Nov 7, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    278
    Registration Numbers
    278
    Same Product Code
    35
    Applicant Total
    2
    Review Days
    96

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    Basic Information

    Device Name
    DITTMAR POWER LIFTER
    K Number
    K883260
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.6990
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Dittmar and Penn Corp.
    Date Received
    August 3, 1988
    Decision Date
    November 7, 1988
    Product Code
    FOX
    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
    FOX Stand, Infusion

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    Other Clearances by Dittmar and Penn Corp.

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    K864953 WEIGHMOBILE, IN BED PATIENT WEIGHING SCALE