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

    NEO-CARE DUAL LUMEN UMBILICAL CATHETER

    K Number: K963972 · Decision Dec 24, 1996
    View on FDA
    Classifications
    1
    FEI Numbers
    16
    Registration Numbers
    17
    Same Product Code
    33
    Applicant Total
    5
    Review Days
    82

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    Basic Information

    Device Name
    NEO-CARE DUAL LUMEN UMBILICAL CATHETER
    K Number
    K963972
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5200
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Klein-Baker Medical, Inc.
    Date Received
    October 3, 1996
    Decision Date
    December 24, 1996
    Product Code
    FOS
    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
    FOS Catheter, Umbilical Artery

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    Other Clearances by Klein-Baker Medical, Inc.

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