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

    THE EXPERIMENTAL

    K Number: K864455 · Decision Mar 18, 1987
    View on FDA
    Classifications
    1
    FEI Numbers
    573
    Registration Numbers
    574
    Same Product Code
    48
    Applicant Total
    1
    Review Days
    126

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    Basic Information

    Device Name
    THE EXPERIMENTAL
    K Number
    K864455
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.6855
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent for Some Indications
    Applicant
    Martin H. Kaufmann
    Date Received
    November 12, 1986
    Decision Date
    March 18, 1987
    Product Code
    EFW
    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
    EFW Toothbrush, Manual

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