Medical Device Manufacturer · GB , Peterlee

Seaward Group - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2018
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.

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