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

    EVIDENT MARK 2 APEX LOCATOR

    K Number: K863834 · Decision Feb 6, 1987
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    6
    Review Days
    129

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    Basic Information

    Device Name
    EVIDENT MARK 2 APEX LOCATOR
    K Number
    K863834
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Pulpdent Corp. of America
    Date Received
    September 30, 1986
    Decision Date
    February 6, 1987
    Advisory Committee
    Unknown
    Review Advisory Committee
    DE
    Third Party
    N

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