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510(k) Data Aggregation

    K Number
    DEN240064
    Device Name
    CT-132
    Date Cleared
    2025-04-11

    (150 days)

    Product Code
    Regulation Number
    882.5806
    Why did this record match?
    Product Code :

    SEE

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