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