Cothera, LLC
Country not established
- Devices
- 1
What Cothera, LLC makes
Cothera, LLC manufactures the VPULSE, a medical device designed for non-invasive monitoring of cardiac function, specifically targeting real-time pulse wave analysis to assess vascular health and blood pressure dynamics.
The VPULSE is classified as a Class II device under FDA regulations and is authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Vpulse Ref K122640
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cothera, LLC have in the registry?
The registry currently lists 1 device for Cothera, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cothera, LLC's devices?
Among its 1 most recently registered device, Cothera, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Cothera, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cothera, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cothera, LLC in the registry?
The most recently registered devices listed for Cothera, LLC include VPULSE.