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

    BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER

    K Number: K072008 · Decision Oct 3, 2007
    View on FDA
    Classifications
    1
    FEI Numbers
    125
    Registration Numbers
    125
    Same Product Code
    190
    Applicant Total
    5
    Review Days
    72

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    Basic Information

    Device Name
    BRAEMAR ER900 WIRELESS SERIES ARRHYTHMIA EVENT RECORDER
    K Number
    K072008
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2910
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Braemar, Inc.
    Date Received
    July 23, 2007
    Decision Date
    October 3, 2007
    Product Code
    DRG
    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
    DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

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