BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    FLORIDA PROBE

    K Number: K875076 · Decision Mar 10, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    159
    Registration Numbers
    159
    Same Product Code
    8
    Applicant Total
    2
    Review Days
    92

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    Basic Information

    Device Name
    FLORIDA PROBE
    K Number
    K875076
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4565
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Florida Probe Corp.
    Date Received
    December 9, 1987
    Decision Date
    March 10, 1988
    Product Code
    EIX
    Advisory Committee
    Dental
    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
    EIX Probe, Periodontic

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    Other Clearances by Florida Probe Corp.

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