BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

    DENTAL-QUECKSILBER (DENTAL MERCURY)

    K Number: K902388 · Decision Jun 28, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    8
    Registration Numbers
    8
    Same Product Code
    3
    Applicant Total
    33
    Review Days
    29

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    Basic Information

    Device Name
    DENTAL-QUECKSILBER (DENTAL MERCURY)
    K Number
    K902388
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.3070
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Degussa AG
    Date Received
    May 30, 1990
    Decision Date
    June 28, 1990
    Product Code
    ELY
    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
    ELY Mercury

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