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

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

    K Number: K071526 · Decision Dec 10, 2008
    View on FDA
    Classifications
    1
    FEI Numbers
    130
    Registration Numbers
    130
    Same Product Code
    504
    Applicant Total
    27
    Review Days
    555

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    Basic Information

    Device Name
    UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMV
    K Number
    K071526
    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
    June 4, 2007
    Decision Date
    December 10, 2008
    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
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    K091238 UNI-VENT-731 SERIES VENTILATORS, MODEL 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
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