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510(k) Data Aggregation

    K Number
    K951848
    Device Name
    AIA-PACK CPR ASSAY
    Manufacturer
    TOSOH MEDICS, INC.
    Date Cleared
    1996-02-13

    (298 days)

    Product Code
    JKD
    Regulation Number
    862.1135
    Why did this record match?
    Product Code :

    JKD

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