Seaward Group
United KingdomFDA applicant, unverified
- Devices
- 1
What Seaward Group makes
The company manufactures the UniPulse, a device designed for pulse measurement and analysis, likely used in medical diagnostics or patient monitoring.
The UniPulse is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
UniPulse Ref K182905
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Seaward Group have in the registry?
The registry currently lists 1 device for Seaward Group. Devices recorded under merged duplicate company entries are counted once.
Which registries list Seaward Group's devices?
Among its 1 most recently registered device, Seaward Group has devices listed in FDA 510(k) (1 device).
What risk classes do Seaward Group's devices fall under?
Among its 1 most recently registered device, the classes recorded for Seaward Group's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Seaward Group in the registry?
The most recently registered devices listed for Seaward Group include UniPulse.