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

    DW232 #31

    K Number: K932774 · Decision Oct 20, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    42
    Registration Numbers
    42
    Same Product Code
    626
    Applicant Total
    2
    Review Days
    134

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    Basic Information

    Device Name
    DW232 #31
    K Number
    K932774
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3060
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Invoclar North America, Inc.
    Date Received
    June 8, 1993
    Decision Date
    October 20, 1993
    Product Code
    EJT
    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
    EJT Alloy, Gold-Based Noble Metal

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    Other Clearances by Invoclar North America, Inc.

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    K920560 DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL