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

    PERMALUX VISIBLE CURE COMPOSITE RESTOR

    K Number: K831351 · Decision Nov 14, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    204
    Registration Numbers
    204
    Same Product Code
    931
    Applicant Total
    6
    Review Days
    203

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    Basic Information

    Device Name
    PERMALUX VISIBLE CURE COMPOSITE RESTOR
    K Number
    K831351
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3690
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Lares Manufacturing Co., Inc.
    Date Received
    April 25, 1983
    Decision Date
    November 14, 1983
    Product Code
    EBF
    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
    EBF Material, Tooth Shade, Resin

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