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

    BEAM LIMITING DEVICE

    K Number: K828605 · Decision Jan 3, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    5
    Review Days
    35

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    Basic Information

    Device Name
    BEAM LIMITING DEVICE
    K Number
    K828605
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Rinn Corp.
    Date Received
    November 29, 1982
    Decision Date
    January 3, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    RA
    Third Party
    N

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    K772313 X-RAY CO-ORDINATOR