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

    DISC-O-AID

    K Number: K821903 · Decision Jul 20, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    282
    Registration Numbers
    282
    Same Product Code
    17
    Applicant Total
    1
    Review Days
    22

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    Basic Information

    Device Name
    DISC-O-AID
    K Number
    K821903
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.5050
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    M. Dahm International Aps
    Date Received
    June 28, 1982
    Decision Date
    July 20, 1982
    Product Code
    IKX
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    PM
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IKX Aid, Transfer

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