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510(k) Data Aggregation

    K Number
    K193005
    Device Name
    DIMI RRT System
    Date Cleared
    2020-08-28

    (305 days)

    Product Code
    Regulation Number
    876.5860
    Why did this record match?
    Applicant Name (Manufacturer) :

    Dialco Medical Inc.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    for the indications for use stated in the enclosure
    Device Description
    Not Found
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