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510(k) Data Aggregation

    K Number
    K970441
    Device Name
    K-KLOSURE 2 INCH LENGTH/4 INCH LENGTH/8 INCH LENGTH/12 INCH LENGTH
    Date Cleared
    1997-05-09

    (93 days)

    Product Code
    Regulation Number
    880.5240
    Why did this record match?
    Applicant Name (Manufacturer) :

    MEDI-FLEX HOSPITAL PRODUCTS, INC.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K962740
    Device Name
    DERMISTICK SEPP APPLICATOR(200 CT)/(40 CT) 260640/260641
    Date Cleared
    1996-09-06

    (53 days)

    Product Code
    Regulation Number
    880.5090
    Why did this record match?
    Applicant Name (Manufacturer) :

    MEDI-FLEX HOSPITAL PRODUCTS, 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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