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

    BAR & RIDER, SCREWS, TUBES

    K Number: K790078 · Decision Feb 27, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    6
    Applicant Total
    5
    Review Days
    48

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    Basic Information

    Device Name
    BAR & RIDER, SCREWS, TUBES
    K Number
    K790078
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    872.6710
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Eurodent, Inc.
    Date Received
    January 10, 1979
    Decision Date
    February 27, 1979
    Product Code
    ECG
    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
    ECG Sterilizer, Boiling Water

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