Gavon, Inc.
Country not established
- Devices
- 1
What Gavon, Inc. makes
Gavon, Inc. manufactures the PORTAPULSE, a portable device designed for monitoring or delivering specific physiological signals or interventions, such as pulse or cardiac output, in ambulatory or clinical settings.
The PORTAPULSE is classified as a Class II medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Portapulse Ref K812131
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gavon, Inc. have in the registry?
The registry currently lists 1 device for Gavon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gavon, Inc.'s devices?
Among its 1 most recently registered device, Gavon, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Gavon, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gavon, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gavon, Inc. in the registry?
The most recently registered devices listed for Gavon, Inc. include PORTAPULSE.