Surepulse Medical Limited is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Surepulse Medical Limited - FDA 510(k) Cleared Devices
Recent clearances: VS Newborn Heart Rate Monitor
1
Total
1
Cleared
0
Denied
Surepulse Medical Limited has 1 FDA 510(k) cleared medical devices. Based in Nottingham, GB.
Last cleared in 2021. Active since 2021. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Surepulse Medical Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Acknowledge Regulatory Strategies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Surepulse Medical Limited
1 devices