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

    QUANTUM 2000 ANGIODYNOGRAPH ULTRASOUND SYSTEM

    K Number: K904019 · Decision Mar 22, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    348
    Registration Numbers
    349
    Same Product Code
    892
    Applicant Total
    5
    Review Days
    204

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    Basic Information

    Device Name
    QUANTUM 2000 ANGIODYNOGRAPH ULTRASOUND SYSTEM
    K Number
    K904019
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1560
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Quantum Medical Systems, Inc.
    Date Received
    August 30, 1990
    Decision Date
    March 22, 1991
    Product Code
    IYO
    Advisory Committee
    Radiology
    Review Advisory Committee
    RA
    Third Party
    N

    Classifications

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

    Product Code Device Name
    IYO System, Imaging, Pulsed Echo, Ultrasonic

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