Circadia Technologies, Ltd.
United KingdomFDA applicant, unverified
- Devices
- 2
What Circadia Technologies, Ltd. makes
Circadia Technologies, Ltd. manufactures the C200 System, a medical device for respiratory monitoring, and the C100 Contactless Breathing Monitor, designed to track breathing patterns without physical contact.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
The Circadia C200 System Ref K234003
Regimes: 510(k) Registry: 510(k)The C100 Contactless Breathing Monitor Ref K200445
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Circadia Technologies, Ltd. have in the registry?
The registry currently lists 2 devices for Circadia Technologies, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Circadia Technologies, Ltd.'s devices?
Among its 2 most recently registered devices, Circadia Technologies, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Circadia Technologies, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Circadia Technologies, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Circadia Technologies, Ltd. in the registry?
The most recently registered devices listed for Circadia Technologies, Ltd. include The Circadia C200 System and The C100 Contactless Breathing Monitor.