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

    DIGITAL TRANSTELEPHONIC ECG MONITORING SYSTEM

    K Number: K892370 · Decision Aug 28, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    80
    Registration Numbers
    80
    Same Product Code
    296
    Applicant Total
    1
    Review Days
    144

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    Basic Information

    Device Name
    DIGITAL TRANSTELEPHONIC ECG MONITORING SYSTEM
    K Number
    K892370
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2920
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Bio-Focus, Inc.
    Date Received
    April 6, 1989
    Decision Date
    August 28, 1989
    Product Code
    DXH
    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
    DXH Transmitters And Receivers, Electrocardiograph, Telephone

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