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

    OMNI-TRAK PATIENT MONITORING SYSTEM

    K Number: K955045 · Decision Jul 11, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    177
    Registration Numbers
    177
    Same Product Code
    574
    Applicant Total
    14
    Review Days
    251

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    Basic Information

    Device Name
    OMNI-TRAK PATIENT MONITORING SYSTEM
    K Number
    K955045
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2340
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Invivo Research, Inc.
    Date Received
    November 3, 1995
    Decision Date
    July 11, 1996
    Product Code
    DPS
    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
    DPS Electrocardiograph

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