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

    SCANNER, ULTRASOUND BODY/HEART

    K Number: K760223 · Decision Sep 7, 1976
    View on FDA
    Classifications
    0
    FEI Numbers
    0
    Registration Numbers
    0
    Same Product Code
    0
    Applicant Total
    1
    Review Days
    57

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    Basic Information

    Device Name
    SCANNER, ULTRASOUND BODY/HEART
    K Number
    K760223
    Clearance Type
    Traditional
    Decision
    Substantially Equivalent
    Applicant
    Mediscra, Inc.
    Date Received
    July 12, 1976
    Decision Date
    September 7, 1976
    Advisory Committee
    Unknown
    Review Advisory Committee
    CV
    Third Party
    N