Sanguina, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Sanguina, LLC makes
Sanguina, LLC manufactures the AnemoCheck, a device designed for assessing respiratory flow and airflow obstruction in clinical settings.
The AnemoCheck is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
AnemoCheck Home Ref K221508
Regimes: 510(k) Registry: 510(k)AnemoCheck Ref K163215
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sanguina, LLC have in the registry?
The registry currently lists 2 devices for Sanguina, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sanguina, LLC's devices?
Among its 2 most recently registered devices, Sanguina, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Sanguina, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Sanguina, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sanguina, LLC in the registry?
The most recently registered devices listed for Sanguina, LLC include AnemoCheck Home and AnemoCheck.