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

    FLORIDA PROBE PERIODONTAL PROBE

    K Number: K890493 · Decision Mar 13, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    139
    Registration Numbers
    139
    Same Product Code
    7
    Applicant Total
    2
    Review Days
    41

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    Basic Information

    Device Name
    FLORIDA PROBE PERIODONTAL PROBE
    K Number
    K890493
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4565
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Florida Probe Corp.
    Date Received
    January 31, 1989
    Decision Date
    March 13, 1989
    Product Code
    EIL
    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
    EIL Gauge, Depth, Instrument, Dental

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    Other Clearances by Florida Probe Corp.

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