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510(k) Data Aggregation

    K Number
    K972957
    Device Name
    SA-EF MULTI-LUMEN EXTENSION SET
    Date Cleared
    1997-09-29

    (49 days)

    Product Code
    Regulation Number
    880.5440
    Why did this record match?
    Applicant Name (Manufacturer) :

    VLV ASSOCIATES, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    The SA.ER Multi-Lumen Extension Sets are to be used for the intravascular system.
    Device Description
    SA.EF Multi-Lumen Extension Set
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    K Number
    K964876
    Device Name
    SA.EF(TM) INFUSION PORT II - CONNECTOR AND EXTENSION SET
    Date Cleared
    1997-02-28

    (85 days)

    Product Code
    Regulation Number
    880.5440
    Why did this record match?
    Applicant Name (Manufacturer) :

    VLV ASSOCIATES, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K955783
    Device Name
    VLV SA.EF INFUSION PORT EXTENSION SETS
    Date Cleared
    1996-02-07

    (48 days)

    Product Code
    Regulation Number
    880.5440
    Why did this record match?
    Applicant Name (Manufacturer) :

    VLV ASSOCIATES, INC.

    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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