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

    NOVA DIAMOND

    K Number: K885233 · Decision Feb 13, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    114
    Registration Numbers
    114
    Same Product Code
    20
    Applicant Total
    2
    Review Days
    55

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    Basic Information

    Device Name
    NOVA DIAMOND
    K Number
    K885233
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4535
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Microcopy, Div. Neo-Flo, Inc.
    Date Received
    December 20, 1988
    Decision Date
    February 13, 1989
    Product Code
    DZP
    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
    DZP Instrument, Diamond, Dental

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