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

    ACUSON S319 TRANSDUCER

    K Number: K862159 · Decision Jul 24, 1986
    View on FDA
    Classifications
    1
    FEI Numbers
    16
    Registration Numbers
    16
    Same Product Code
    71
    Applicant Total
    24
    Review Days
    48

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    Basic Information

    Device Name
    ACUSON S319 TRANSDUCER
    K Number
    K862159
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2880
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Acuson Computed Sonography
    Date Received
    June 6, 1986
    Decision Date
    July 24, 1986
    Product Code
    JOP
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    JOP Transducer, Ultrasonic

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    Other Clearances by Acuson Computed Sonography

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    K874363 ACUSON S228 AND S328 TRANSDUCERS FOR ABDOM. APPLI.
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