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

    ARGILITE 4 GOLD ALLOY FOR PORCELAIN

    K Number: K903686 · Decision Aug 29, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    128
    Registration Numbers
    129
    Same Product Code
    25
    Applicant Total
    217
    Review Days
    16

    Basic Information

    Device Name
    ARGILITE 4 GOLD ALLOY FOR PORCELAIN
    K Number
    K903686
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.3520
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    ARGEN PRECIOUS METALS, INC.
    Date Received
    August 13, 1990
    Decision Date
    August 29, 1990
    Product Code
    EFT
    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
    EFT Cleanser, Denture, Over The Counter

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