CorVent Medical’s Respond Ventilator Gets FDA Nod
CorVent Medical’s Respond ventilator, designed for pediatric to adult patients, has received FDA 510(k) clearance as the first U.S.-manufactured ventilator cleared in over 20 years.
CorVent Medical’s Respond ventilator, designed for pediatric to adult patients, has received FDA 510(k) clearance as the first U.S.-manufactured ventilator cleared in over 20 years.
DHL, XRP Healthcare and The Burnratty Investment Group have partnered to transport Spiritus Vitality ventilators to facilities in Uganda.
ReddyPort announced that the FDA granted 510(k) premarket clearance for the company’s non-invasive ventilation device (NIV).
CorVent Medical’s Respond ventilator, designed for pediatric to adult patients, has received FDA 510(k) clearance as the first U.S.-manufactured ventilator cleared in over 20 years.
Philips Respironics recalled certain reworked ventilators for issues related to foam adhesion failure and foam debris.
Read MoreThe FDA is providing additional information to patients, caregivers, and healthcare providers about two recent issues in certain ventilators.
Read MoreA team of engineers from MIT are developing a ventilator solution that will aid people with compromised diaphragm function.
Read MorePhilips’ ventilator recall woes, which stemmed from the machines causing patient health issues, are under investigation by French prosecutors.
Read MoreHamilton Medical AG is recalling an intensive care ventilator after complaints revealed a hardware issue with its status indicator board.
Read MoreGetinge is recalling several different types of ventilators in its device portfolio that are being labeled as a Class I event by the FDA.
Read MoreBreas Medical USA announced the release and immediate availability of the Xpac by Breas extended life battery for ventilators.