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

    SONY VIDEO GRAPHIC PRINTER UP-850

    K Number: K890826 · Decision Mar 14, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    193
    Registration Numbers
    193
    Same Product Code
    17
    Applicant Total
    2
    Review Days
    25

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    Basic Information

    Device Name
    SONY VIDEO GRAPHIC PRINTER UP-850
    K Number
    K890826
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    878.4160
    Medical Specialty
    General, Plastic Surgery
    Decision
    Substantially Equivalent
    Applicant
    Sony Corp. of America
    Date Received
    February 17, 1989
    Decision Date
    March 14, 1989
    Product Code
    KQM
    Advisory Committee
    General, Plastic Surgery
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    KQM Camera, Surgical And Accessories

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