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

    KONTRON SIGMA 44 HVCD ULTRASOUND IMAGING SYSTEM

    K Number: K896437 · Decision Dec 3, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    18
    Registration Numbers
    18
    Same Product Code
    47
    Applicant Total
    57
    Review Days
    389

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    Basic Information

    Device Name
    KONTRON SIGMA 44 HVCD ULTRASOUND IMAGING SYSTEM
    K Number
    K896437
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2120
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Kontron Instruments, Inc.
    Date Received
    November 9, 1989
    Decision Date
    December 3, 1990
    Product Code
    DPT
    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
    DPT Probe, Blood-Flow, Extravascular

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