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

    BIOCOR 200 HIGH PERFORMANCEOXYGENATOR

    K Number: K964967 · Decision Mar 6, 1997
    View on FDA
    Classifications
    1
    FEI Numbers
    31
    Registration Numbers
    31
    Same Product Code
    253
    Applicant Total
    33
    Review Days
    86

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    Basic Information

    Device Name
    BIOCOR 200 HIGH PERFORMANCEOXYGENATOR
    K Number
    K964967
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    870.4350
    Medical Specialty
    Cardiovascular
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Minntech Corp.
    Date Received
    December 10, 1996
    Decision Date
    March 6, 1997
    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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