Severn Research, Inc.
Country not established
- Devices
- 1
What Severn Research, Inc. makes
Severn Research, Inc. manufactures a breast simulation system designed for medical training and procedural practice, replicating anatomical structures for realistic simulation purposes.
The breast simulation system is classified as a Class II medical device in the US and is authorised via the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Breast Simulation System Ref K925714
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Severn Research, Inc. have in the registry?
The registry currently lists 1 device for Severn Research, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Severn Research, Inc.'s devices?
Among its 1 most recently registered device, Severn Research, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Severn Research, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Severn Research, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Severn Research, Inc. in the registry?
The most recently registered devices listed for Severn Research, Inc. include BREAST SIMULATION SYSTEM.