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

    PLEXUS 2 & 3.5 HOLLOW FIBER OXYGENATORS

    K Number: K931444 · Decision May 27, 1994
    View on FDA
    Classifications
    1
    FEI Numbers
    31
    Registration Numbers
    31
    Same Product Code
    253
    Applicant Total
    20
    Review Days
    431

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    Basic Information

    Device Name
    PLEXUS 2 & 3.5 HOLLOW FIBER OXYGENATORS
    K Number
    K931444
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4350
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Sorin Biomedica, Fiat, USA, Inc.
    Date Received
    March 22, 1993
    Decision Date
    May 27, 1994
    Product Code
    DTZ
    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
    DTZ Oxygenator, Cardiopulmonary Bypass

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