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

    CHANNEL BACK

    K Number: K823093 · Decision Nov 16, 1982
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    27

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    Basic Information

    Device Name
    CHANNEL BACK
    K Number
    K823093
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    J.G. Shuman Assoc.
    Date Received
    October 20, 1982
    Decision Date
    November 16, 1982
    Advisory Committee
    Unknown
    Review Advisory Committee
    PM
    Third Party
    N