Demasq Limited is one of 491 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Demasq Limited - FDA 510(k) Cleared Devices
Recent clearances: DEMASQ IMAGING SPFTWARE DEVICE
1
Total
1
Cleared
0
Denied
Demasq Limited has 1 FDA 510(k) cleared medical devices. Based in Cardiff Wales, GB.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Demasq Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Demasq Limited
1 devices