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

    COATED APEX PROBE

    K Number: K890735 · Decision Apr 19, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    49
    Registration Numbers
    49
    Same Product Code
    45
    Applicant Total
    9
    Review Days
    65

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    Basic Information

    Device Name
    COATED APEX PROBE
    K Number
    K890735
    Device Class
    FDA unclassified
    Clearance Type
    Traditional
    Medical Specialty
    Unknown
    Decision
    Substantially Equivalent
    Applicant
    Analytic Technology
    Date Received
    February 13, 1989
    Decision Date
    April 19, 1989
    Product Code
    LQY
    Advisory Committee
    Unknown
    Review Advisory Committee
    DE
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LQY Locator, Root Apex

    Similar 510(k) Clearances

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    Apex Locator

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    Apex Locator (AL-Pex), Apex Locator (AL-Pex+)

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    FDA Unclassified ·Unknown

    Root Apex Locator

    FDA 510(k)
    FDA Unclassified ·Unknown
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    K832179 HOT PROBE MODEL 6001
    K823486 TOUCH-N-HEAT MODEL 5001
    K820598 HOT & COLD PULP TESTER #4001
    K801974 ANALYTIC TECH. METAL POINT HEATER #3001
    K790799 PULPTESTER MODEL 2001