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

    DISPOSABLE DENTAL PROBE/EXPLORER

    K Number: K880590 · Decision Mar 2, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    99
    Registration Numbers
    99
    Same Product Code
    71
    Applicant Total
    505
    Review Days
    20

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    Basic Information

    Device Name
    DISPOSABLE DENTAL PROBE/EXPLORER
    K Number
    K880590
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4565
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Baxter Healthcare Corp
    Date Received
    February 11, 1988
    Decision Date
    March 2, 1988
    Product Code
    EKJ
    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
    EKJ Burnisher, Operative

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