Isansys Lifecare, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Isansys Lifecare, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Patient Status Engine
1
Total
1
Cleared
0
Denied
Isansys Lifecare, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Oxford, GB.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Isansys Lifecare, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Isansys Lifecare, Ltd.
1 devices