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

    DIGIDENT ELEKTRONIC APEX LOCATOR

    K Number: K832118 · Decision Sep 26, 1983
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    88

    Basic Information

    Device Name
    DIGIDENT ELEKTRONIC APEX LOCATOR
    K Number
    K832118
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    ORA-MUSZERIPARI SZOVETKEZET
    Date Received
    June 30, 1983
    Decision Date
    September 26, 1983
    Advisory Committee
    Unknown
    Review Advisory Committee
    SU
    Third Party
    N