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

    COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM

    K Number: K902926 · Decision Nov 26, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    398
    Registration Numbers
    399
    Same Product Code
    408
    Applicant Total
    71
    Review Days
    146

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    Basic Information

    Device Name
    COLOR VELOCITY IMAGING (CVI) OPTION FOR PLATINUM
    K Number
    K902926
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1570
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Philips Medical Systems North America, Inc.
    Date Received
    July 3, 1990
    Decision Date
    November 26, 1990
    Product Code
    ITX
    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
    ITX Transducer, Ultrasonic, Diagnostic

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