Remote Diagnostic Technologies Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Remote Diagnostic Technologies Limited - FDA 510(k) Cleared Devices
Recent clearances: Tempus Pro Patient Monitor
1
Total
1
Cleared
0
Denied
Remote Diagnostic Technologies Limited has 1 FDA 510(k) cleared medical devices. Based in Basingstoke, GB.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Remote Diagnostic Technologies Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Philips North America, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Remote Diagnostic Technologies Limited
1 devices