BEUDAMED
    FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

    ABG KITS - CMS 4000 SERIES

    K Number: K830333 · Decision Mar 31, 1983
    View on FDA
    Classifications
    1
    FEI Numbers
    39
    Registration Numbers
    39
    Same Product Code
    57
    Applicant Total
    13
    Review Days
    58

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    Basic Information

    Device Name
    ABG KITS - CMS 4000 SERIES
    K Number
    K830333
    Device Class
    FDA class 1
    Clearance Type
    Traditional
    Regulation Number
    868.1100
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Currie Medical Specialties, Inc.
    Date Received
    February 1, 1983
    Decision Date
    March 31, 1983
    Product Code
    CBT
    Advisory Committee
    Anesthesiology
    Review Advisory Committee
    AN
    Third Party
    N

    Classifications

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

    Product Code Device Name
    CBT Arterial Blood Sampling Kit

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