Prosum Medical Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Prosum Medical Limited - FDA 510(k) Cleared Devices
Recent clearances: Small Volume 0.2mL Syringe
1
Total
1
Cleared
0
Denied
Prosum Medical Limited has 1 FDA 510(k) cleared medical devices. Based in Uxbridge, GB.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Prosum Medical Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kymanox as regulatory consultant.
FDA 510(k) Regulatory Record - Prosum Medical Limited
1 devices