BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent - Subject to Tracking Reg. 🇺🇸 United States

    PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTION

    K Number: K001646 · Decision Oct 20, 2000
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    504
    Applicant Total
    110
    Review Days
    143

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    Basic Information

    Device Name
    PURITAN-BENNETT 840 VENTILATOR SYSTEM WITH NEOMODE OPTION
    K Number
    K001646
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5895
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent - Subject to Tracking Reg.
    Applicant
    Puritan Bennett Corp.
    Date Received
    May 30, 2000
    Decision Date
    October 20, 2000
    Product Code
    CBK
    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
    CBK Ventilator, Continuous, Facility Use

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