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510(k) Data Aggregation

    K Number
    K133779
    Device Name
    CP RELIEF WAND
    Date Cleared
    2014-05-30

    (169 days)

    Product Code
    Regulation Number
    882.5890
    Why did this record match?
    Applicant Name (Manufacturer) :

    MID-AMERICA MEDICAL INNOVATIONS, LLC.

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