Prosys International, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Prosys International, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Avantgarde Faecal Management Systems, Avantgarde Faecal Management System Replacement Pouches
1
Total
1
Cleared
0
Denied
Prosys International, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Wimbledon, GB.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Prosys International, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Prosys International, Ltd.
1 devices