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

    MOBILECARE MONITOR

    K Number: K122333 · Decision Nov 19, 2012
    View on FDA
    Classifications
    1
    FEI Numbers
    125
    Registration Numbers
    125
    Same Product Code
    190
    Applicant Total
    2
    Review Days
    109

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    Basic Information

    Device Name
    MOBILECARE MONITOR
    K Number
    K122333
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.2910
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Aframe Digital, Inc.
    Date Received
    August 2, 2012
    Decision Date
    November 19, 2012
    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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    Other Clearances by Aframe Digital, Inc.

    K Number Device Name
    K090138 MOBILECARE MONITOR, MODEL 2100