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510(k) Data Aggregation

    K Number
    K954999
    Device Name
    LILY MULTICANNULA GUIDE
    Date Cleared
    1996-04-04

    (155 days)

    Product Code
    Regulation Number
    876.1075
    Why did this record match?
    Applicant Name (Manufacturer) :

    LILY IMAGING SOLUTIONS CO.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K954998
    Device Name
    LILY DARK VIEWER
    Date Cleared
    1996-01-29

    (89 days)

    Product Code
    Regulation Number
    892.1890
    Why did this record match?
    Applicant Name (Manufacturer) :

    LILY IMAGING SOLUTIONS CO.

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

    Ask a specific question about this device

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