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510(k) Data Aggregation

    K Number
    K001121
    Device Name
    OXYGEN APPLIED SYMPTOM IMPROVEMENT SYSTEM (OASIS)
    Manufacturer
    ENGINEERED MEDICAL TECHNOLOGY, INC.
    Date Cleared
    2001-11-29

    (601 days)

    Product Code
    CBF
    Regulation Number
    868.5470
    Why did this record match?
    Applicant Name (Manufacturer) :

    ENGINEERED MEDICAL TECHNOLOGY, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
    Intended Use
    Device Description
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