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

    LINEAR ARRAY TRANSDUCER OR SCANHEAD

    K Number: K840408 · Decision Apr 25, 1984
    View on FDA
    Classifications
    1
    FEI Numbers
    348
    Registration Numbers
    349
    Same Product Code
    892
    Applicant Total
    10
    Review Days
    85

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    Basic Information

    Device Name
    LINEAR ARRAY TRANSDUCER OR SCANHEAD
    K Number
    K840408
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1560
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Applicant
    Adr Ultrasound
    Date Received
    January 31, 1984
    Decision Date
    April 25, 1984
    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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