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510(k) Data Aggregation

    K Number
    DEN240048
    Device Name
    Spur Peripheral Retrievable Stent System
    Manufacturer
    Reflow Medical, Inc.
    Date Cleared
    2025-05-29

    (251 days)

    Product Code
    SEU
    Regulation Number
    870.5110
    Why did this record match?
    Product Code :

    SEU

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