BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE

    K Number: K900560 · Decision Dec 3, 1990
    View on FDA
    Classifications
    1
    FEI Numbers
    10
    Registration Numbers
    10
    Same Product Code
    17
    Applicant Total
    37
    Review Days
    299

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    Basic Information

    Device Name
    ACUSON HEARTSOUND/PULSE/RESPIRATION MODULE
    K Number
    K900560
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    870.2390
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Acuson Corp.
    Date Received
    February 7, 1990
    Decision Date
    December 3, 1990
    Product Code
    DQC
    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
    DQC Phonocardiograph

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