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    K Number
    K050788
    Device Name
    EVERLIFE
    Manufacturer
    EVERLIFE MEDICAL INSTRUMENT CO., LTD.
    Date Cleared
    2005-05-13

    (46 days)

    Product Code
    GXY
    Regulation Number
    882.1320
    Why did this record match?
    Applicant Name (Manufacturer) :

    EVERLIFE MEDICAL INSTRUMENT CO., LTD.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Intended to be applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation.
    Device Description
    EVERLIFE, Various Models of Self Adhesive Electrodes, AP series
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