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

    DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020, GI VERSION

    K Number: K920664 · Decision Dec 23, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    31
    Registration Numbers
    31
    Same Product Code
    68
    Applicant Total
    16
    Review Days
    679

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    Basic Information

    Device Name
    DIAGNOSTIC ULTRASOUND/URO-GYN UPS 2020, GI VERSION
    K Number
    K920664
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1725
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Diagnostic Ultrasound Corp.
    Date Received
    February 13, 1992
    Decision Date
    December 23, 1993
    Product Code
    FFX
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    GU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    FFX System, Gastrointestinal Motility (Electrical)

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