Intersurgical , Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Intersurgical , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: TNI Clear-Guard™ 3 angled breathing filter (1545020)
1
Total
1
Cleared
0
Denied
Intersurgical , Ltd. has 1 FDA 510(k) cleared medical devices. Based in Berkshire, GB.
Last cleared in 2023. Active since 2023. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Intersurgical , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intersurgical Incorporated as regulatory consultant.
FDA 510(k) Regulatory Record - Intersurgical , Ltd.
1 devices