Shots:
- The US FDA has permitted marketing of a device intended for the temporary reduction of sleep disturbance related to nightmares in patients aged ≥22 yrs. suffering from nightmare disorder or PTSD
- Nightware utilizes Apple Watch and an iPhone that is configured and logged into a software application and the Nightware server and monitors the wearer’s HR and movement while they sleep and if they are having a nightmare, gently arouse them out of the dream without waking up completely, using the smartwatch’s vibrations
- The platform received the US FDA’s BT designation in May’2019 and now is available by prescription only and is intended for home use
Click here to read full press release/ article | Ref: FDA | Image: IT PRO
The post NightWare Receives the US FDA’s Approval for the First Medical Device to Stop NightMAres Related to PTSD first appeared on PharmaShots.
