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510(k) Data Aggregation

    K Number
    K001146
    Device Name
    GENYX FLEXIBLE INJECTION NEEEDLE
    Manufacturer
    Date Cleared
    2000-06-30

    (81 days)

    Product Code
    Regulation Number
    876.1500
    Why did this record match?
    Applicant Name (Manufacturer) :

    GENY MEDICAL, INC.

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