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510(k) Data Aggregation

    K Number
    K010937
    Device Name
    SEP-10S PLUS, AND SP-12S PRO.
    Manufacturer
    Date Cleared
    2001-06-25

    (88 days)

    Product Code
    Regulation Number
    880.5725
    Why did this record match?
    Applicant Name (Manufacturer) :

    VILTECHMEDA

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