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

    DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC

    K Number: K831344 · Decision Jul 18, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    2
    Review Days
    84

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    Basic Information

    Device Name
    DIFFERENTIA/DIAGNOSTIC OCCLUSA/APPLIANC
    K Number
    K831344
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Brimms, Inc.
    Date Received
    April 25, 1983
    Decision Date
    July 18, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    DE
    Third Party
    N

    Other Clearances by Brimms, Inc.

    K Number Device Name
    K842788 DIFFERENTIAL DIAG. OCCLUSAL APPLIANCE