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

    ELASTIC COMPRESSION ANKLET

    K Number: K823789 · Decision Jan 7, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    268
    Registration Numbers
    268
    Same Product Code
    5
    Applicant Total
    1
    Review Days
    22

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    Basic Information

    Device Name
    ELASTIC COMPRESSION ANKLET
    K Number
    K823789
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    880.5780
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Applicant
    Orthopaedic Resources Corp.
    Date Received
    December 16, 1982
    Decision Date
    January 7, 1983
    Product Code
    FQL
    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
    FQL Stocking, Medical Support (For General Medical Purposes)

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