Cambridge Assoc.
Country not established
- Devices
- 1
What Cambridge Assoc. makes
Cambridge Assoc. manufactures the Breathe Fit, a device designed for respiratory support or monitoring, likely intended for use in home or clinical settings to assist with breathing.
The Breathe Fit is classified as a Class I medical device under FDA regulations and is listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Breathe Fit Ref K963326
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cambridge Assoc. have in the registry?
The registry currently lists 1 device for Cambridge Assoc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cambridge Assoc.'s devices?
Among its 1 most recently registered device, Cambridge Assoc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cambridge Assoc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cambridge Assoc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cambridge Assoc. in the registry?
The most recently registered devices listed for Cambridge Assoc. include BREATHE FIT.