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510(k) Data Aggregation

    K Number
    K963059
    Device Name
    SUNQUEST INTERNATIONAL
    Date Cleared
    1996-08-23

    (21 days)

    Product Code
    Regulation Number
    886.5850
    Why did this record match?
    Applicant Name (Manufacturer) :

    SUNQUEST INTL., INC.

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