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510(k) Data Aggregation

    K Number
    K030374
    Device Name
    SONIK LDI 20 AIR
    Manufacturer
    Date Cleared
    2003-08-25

    (202 days)

    Product Code
    Regulation Number
    868.5630
    Why did this record match?
    Applicant Name (Manufacturer) :

    EVIT LABS, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    To be used to convert liquid medication into aerosol for inhalation by patient.
    Device Description
    Not Found
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