This survey is intended to gather insights on a new resuscitation – ventilation device, the fluidIQ HOPE inVent.
The inVent is pending US FDA 510(k) clearance and not currently available for sale. However, please answer these questions if the device were to be FDA cleared and available for use.
Prior to completing the survey questions, please view the Survey Video to gain a better understanding of the device.
Your feedback is extremely important to the continued development of the inVent as well as future availability for providers like yourself or your team.
Completing this survey will take approximately 8 minutes of your time.
Thank you again for taking the time to complete this survey.
The fluidIQ Team
Disclaimer: Pending US FDA 510(k) clearance. Not available for sale in the U.S.
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