BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

    MEDIZIV CENTRAL VEIN CATHETER

    K Number: K884491 · Decision Jun 5, 1989
    View on FDA
    Classifications
    1
    FEI Numbers
    276
    Registration Numbers
    277
    Same Product Code
    889
    Applicant Total
    2
    Review Days
    222

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    Basic Information

    Device Name
    MEDIZIV CENTRAL VEIN CATHETER
    K Number
    K884491
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.1250
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Applicant
    Mediziv Medical Devices, Ltd.
    Date Received
    October 26, 1988
    Decision Date
    June 5, 1989
    Product Code
    DQY
    Advisory Committee
    Cardiovascular
    Review Advisory Committee
    CV
    Third Party
    N

    Classifications

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

    Product Code Device Name
    DQY Catheter, Percutaneous

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    Other Clearances by Mediziv Medical Devices, Ltd.

    K Number Device Name
    K894725 MEDIZIV EPIDURAL SYSTEMS