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

    OMNI-VENT, SERIES D/MRI

    K Number: K881420 · Decision Jun 14, 1988
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    504
    Applicant Total
    2
    Review Days
    71

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    Basic Information

    Device Name
    OMNI-VENT, SERIES D/MRI
    K Number
    K881420
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5895
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Stein-Gates Medical Equipment, Inc.
    Date Received
    April 4, 1988
    Decision Date
    June 14, 1988
    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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    Other Clearances by Stein-Gates Medical Equipment, Inc.

    K Number Device Name
    K872113 OMNI-VENT, SERIES D