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

    UNI-VENT-731 SERIES VENTILATORS, MODEL 731EMV+

    K Number: K091238 · Decision Aug 13, 2009
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    504
    Applicant Total
    27
    Review Days
    108

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    Basic Information

    Device Name
    UNI-VENT-731 SERIES VENTILATORS, MODEL 731EMV+
    K Number
    K091238
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    868.5895
    Medical Specialty
    Anesthesiology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    Impact Instrumentation, Inc.
    Date Received
    April 27, 2009
    Decision Date
    August 13, 2009
    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 Impact Instrumentation, Inc.

    K Number Device Name
    K133196 IMPACT MODEL 323 ASPIRATOR
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    K071526 UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMV
    K051476 UNI-VENT MODEL 73X
    K032386 UNI-VENT MODEL 730AEV (AUTOMATIC EMERGENCY VENTILATOR)
    K022062 IMPACT, UNIVERSAL SINGLE-LIMB, VENTILATOR CIRCUIT, MODEL 820-0099-00
    K951423 ASPIRATOR, CONTINUOUS & PROGRAMMABLE INTERMITTENT
    K941096 ELECTRIC VACUM PUMP
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