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

    PDS-2000

    K Number: K902653 · Decision Sep 13, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    98
    Registration Numbers
    98
    Same Product Code
    4
    Applicant Total
    1
    Review Days
    90

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    Basic Information

    Device Name
    PDS-2000
    K Number
    K902653
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.4565
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Intl. Equipment and Supply Corp.
    Date Received
    June 15, 1990
    Decision Date
    September 13, 1990
    Product Code
    EIK
    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
    EIK Carver, Wax, Dental

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