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

    SERVO VENTILATOR 300

    K Number: K902859 · Decision Apr 26, 1991
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    504
    Applicant Total
    6
    Review Days
    301

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    Basic Information

    Device Name
    SERVO VENTILATOR 300
    K Number
    K902859
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5895
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Applicant
    Siemens Life Support Systems
    Date Received
    June 29, 1990
    Decision Date
    April 26, 1991
    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 Siemens Life Support Systems

    K Number Device Name
    K903991 PCM ANESTHESIA
    K901474 ANESTHESIA WORKSTATION
    K893786 SERVO ANESTHESIA CIRCLE 985
    K890932 CAV 3.0C SOFTWARE PROGRAM
    K890921 DATA EXCHANGE SYSTEM, MODEL 24