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

    MIZZY SYRIJET MARK IV

    K Number: K790193 · Decision Apr 23, 1979
    View on FDA
    Classifications
    1
    FEI Numbers
    3
    Registration Numbers
    3
    Same Product Code
    10
    Applicant Total
    1
    Review Days
    87

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    Basic Information

    Device Name
    MIZZY SYRIJET MARK IV
    K Number
    K790193
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    872.4475
    Medical Specialty
    Dental
    Decision
    Substantially Equivalent
    Applicant
    Mizzy, Inc.
    Date Received
    January 26, 1979
    Decision Date
    April 23, 1979
    Product Code
    EGM
    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
    EGM Injector, Jet, Mechanical-Powered

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