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

    INTRICON DATRIX SIRONA EVENT/ HOLTER RECORDER

    K Number: K112601 · Decision Nov 9, 2011
    View on FDA
    Classifications
    1
    FEI Numbers
    48
    Registration Numbers
    48
    Same Product Code
    59
    Applicant Total
    2
    Review Days
    63

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    Basic Information

    Device Name
    INTRICON DATRIX SIRONA EVENT/ HOLTER RECORDER
    K Number
    K112601
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2800
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Intricon Datrix Corporation
    Date Received
    September 7, 2011
    Decision Date
    November 9, 2011
    Product Code
    MWJ
    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
    MWJ Electrocardiograph, Ambulatory (Without Analysis)

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    Other Clearances by Intricon Datrix Corporation

    K Number Device Name
    K111160 INTRICON DATRIX CENTAURI MT AMBULATORY PATIENT ECG TELEMETRY SYSTEM (APETS)