Circadia Technologies, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Circadia Technologies, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: The Circadia C200 System, The C100 Contactless Breathing Monitor
2
Total
2
Cleared
0
Denied
Circadia Technologies, Ltd. has 2 FDA 510(k) cleared medical devices. Based in Croydon, GB.
Latest FDA clearance: May 2024. Active since 2020. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Circadia Technologies, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Rook Quality Systems, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Circadia Technologies, Ltd.
2 devices