BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    VITA VMK MASTER

    K Number: K093446 · Decision Dec 3, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    158
    Registration Numbers
    158
    Same Product Code
    481
    Applicant Total
    2
    Review Days
    28

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    Basic Information

    Device Name
    VITA VMK MASTER
    K Number
    K093446
    Device Class
    FDA class 2
    Clearance Type
    Special
    Regulation Number
    872.6660
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Vita Zahnfabrik H. Rauter GmbH & Co. Kg.
    Date Received
    November 5, 2009
    Decision Date
    December 3, 2009
    Product Code
    EIH
    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
    EIH Powder, Porcelain

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    Other Clearances by Vita Zahnfabrik H. Rauter GmbH & Co. Kg.

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    K251587 VITA VMLC Primer