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

    B. BRAUN IV START KITS

    K Number: K950184 · Decision Mar 15, 1995
    View on FDA
    Classifications
    1
    FEI Numbers
    68
    Registration Numbers
    68
    Same Product Code
    29
    Applicant Total
    19
    Review Days
    57

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    Basic Information

    Device Name
    B. BRAUN IV START KITS
    K Number
    K950184
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5200
    Medical Specialty
    General Hospital
    Decision
    Unknown
    Statement or Summary
    Summary
    Applicant
    B. Braun of America, Inc.
    Date Received
    January 17, 1995
    Decision Date
    March 15, 1995
    Product Code
    LRS
    Advisory Committee
    General Hospital
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

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

    Product Code Device Name
    LRS I.V. Start Kit

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