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

    HEARTTRACE LEFT VENTRICULAR ANALYSIS SOFTWARE

    K Number: K933073 · Decision Oct 7, 1993
    View on FDA
    Classifications
    1
    FEI Numbers
    123
    Registration Numbers
    123
    Same Product Code
    198
    Applicant Total
    4
    Review Days
    106

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    Basic Information

    Device Name
    HEARTTRACE LEFT VENTRICULAR ANALYSIS SOFTWARE
    K Number
    K933073
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    892.1600
    Medical Specialty
    Radiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Heartware Intl. Corp.
    Date Received
    June 23, 1993
    Decision Date
    October 7, 1993
    Product Code
    IZI
    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
    IZI System, X-Ray, Angiographic

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    Other Clearances by Heartware Intl. Corp.

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