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

    X-BEAM FILM 3TC

    K Number: K833592 · Decision Dec 27, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    76

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    Basic Information

    Device Name
    X-BEAM FILM 3TC
    K Number
    K833592
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Amorient Ent.
    Date Received
    October 12, 1983
    Decision Date
    December 27, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    DE
    Third Party
    N