James P Boyd
Country not established
- Devices
- 1
What James P Boyd makes
James P Boyd manufactures the SNORENTI device, a Class II medical product.
The SNORENTI is regulated under the FDA 510(k) pathway and is listed in the fda_510k registry; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Snorenti Ref K032410
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does James P Boyd have in the registry?
The registry currently lists 1 device for James P Boyd. Devices recorded under merged duplicate company entries are counted once.
Which registries list James P Boyd's devices?
Among its 1 most recently registered device, James P Boyd has devices listed in FDA 510(k) (1 device).
What risk classes do James P Boyd's devices fall under?
Among its 1 most recently registered device, the classes recorded for James P Boyd's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from James P Boyd in the registry?
The most recently registered devices listed for James P Boyd include SNORENTI.