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

    BOGER AUTO-TRACTION DEVICE

    K Number: K820663 · Decision May 3, 1982
    View on FDA
    Classifications
    1
    FEI Numbers
    41
    Registration Numbers
    41
    Same Product Code
    14
    Applicant Total
    1
    Review Days
    54

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    Basic Information

    Device Name
    BOGER AUTO-TRACTION DEVICE
    K Number
    K820663
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    890.5925
    Medical Specialty
    Physical Medicine
    Decision
    Substantially Equivalent
    Applicant
    D.C. Medical Device, Inc.
    Date Received
    March 10, 1982
    Decision Date
    May 3, 1982
    Product Code
    ILZ
    Advisory Committee
    Physical Medicine
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    ILZ Accessories, Traction

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