BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    NIMA (NEEDLELESS INJECTIONSITE MASTER ADAPTER) & I.V. SET

    K Number: K952852 · Decision Feb 16, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    424
    Registration Numbers
    424
    Same Product Code
    1173
    Applicant Total
    6
    Review Days
    240

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    Basic Information

    Device Name
    NIMA (NEEDLELESS INJECTIONSITE MASTER ADAPTER) & I.V. SET
    K Number
    K952852
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5440
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Critical Device Corp.
    Date Received
    June 21, 1995
    Decision Date
    February 16, 1996
    Product Code
    FPA
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    FPA Set, Administration, Intravascular

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    Other Clearances by Critical Device Corp.

    K Number Device Name
    K983926 MPS GRAVITY FLOW CONTROL SET
    K964918 NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER WITH POSIFLOW POSITIVE DISPLACEMENT FEATURE, AND I.V. SETS
    K964989 CDC VIAL AND BAG ACCESS PIN (CDC-P-1/P-2/P-3/P-4/P-5)
    K964812 NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER AND I.V. SET
    K955896 MACROBORE TUBING - CDC-F-1 THROUGH CDC-F-11