Medvision, Inc.
Country not established
- Devices
- 1
What Medvision, Inc. makes
Medvision, Inc. manufactures the Medvision Personal Monitor, a device designed for continuous or intermittent physiological monitoring of patients, likely targeting home or ambulatory use.
The company’s portfolio is regulated under Class II devices in the US, with the Medvision Personal Monitor authorised via the FDA’s 510(k) pathway. The device is listed in the FDA’s 510(k) database.
Catalogue
Medvision Personal Monitor Ref K961343
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medvision, Inc. have in the registry?
The registry currently lists 1 device for Medvision, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medvision, Inc.'s devices?
Among its 1 most recently registered device, Medvision, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medvision, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medvision, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medvision, Inc. in the registry?
The most recently registered devices listed for Medvision, Inc. include MEDVISION PERSONAL MONITOR.