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

    MODEL 200A ELECTRONIC FORCE-SENSING PROBE

    K Number: K884813 · Decision Jan 5, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    139
    Registration Numbers
    139
    Same Product Code
    7
    Applicant Total
    1
    Review Days
    49

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    Basic Information

    Device Name
    MODEL 200A ELECTRONIC FORCE-SENSING PROBE
    K Number
    K884813
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4565
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Vine Valley Research
    Date Received
    November 17, 1988
    Decision Date
    January 5, 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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