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510(k) Data Aggregation

    K Number
    K011176
    Device Name
    REUSABLE GLASS SYRINGES
    Date Cleared
    2001-08-10

    (115 days)

    Product Code
    Regulation Number
    880.5860
    Why did this record match?
    Applicant Name (Manufacturer) :

    LOCKETT MEDICAL CORP.

    AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP AuthorizedThirdparty
    Intended Use
    Device Description
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    K Number
    K954887
    Device Name
    STERILE WATER O.9% STERILE SALINE
    Date Cleared
    1996-01-24

    (100 days)

    Product Code
    Regulation Number
    880.5200
    Why did this record match?
    Applicant Name (Manufacturer) :

    LOCKETT MEDICAL CORP.

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

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