Sensydia, Inc.
Country not established
- Devices
- 1
What Sensydia, Inc. makes
Sensydia, Inc. manufactures the Integrated CardioRespiratory System, a device designed for monitoring and analyzing combined cardiac and respiratory function in clinical settings.
The company’s portfolio is regulated under FDA’s Class II device classification, with the Integrated CardioRespiratory System authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. Sensydia, Inc. is based in the United States.
Catalogue
Integrated CardioRespiratory System Ref K173156
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sensydia, Inc. have in the registry?
The registry currently lists 1 device for Sensydia, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sensydia, Inc.'s devices?
Among its 1 most recently registered device, Sensydia, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sensydia, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sensydia, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sensydia, Inc. in the registry?
The most recently registered devices listed for Sensydia, Inc. include Integrated CardioRespiratory System.