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510(k) Data Aggregation

    K Number
    K131954
    Device Name
    MEDI PEN NEEDLE
    Date Cleared
    2014-05-29

    (336 days)

    Product Code
    Regulation Number
    880.5570
    Why did this record match?
    Applicant Name (Manufacturer) :

    SHANGHAI CARELIFE INTERNATIONAL TRADING CO., LTD.

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