Monox, Inc.
Country not established
- Devices
- 1
What Monox, Inc. makes
Monox, Inc. manufactures the WATCHCHILD, a medical device designed for monitoring and alerting in pediatric patient care settings.
The WATCHCHILD is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Watchchild Ref K893981
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Monox, Inc. have in the registry?
The registry currently lists 1 device for Monox, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Monox, Inc.'s devices?
Among its 1 most recently registered device, Monox, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Monox, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Monox, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Monox, Inc. in the registry?
The most recently registered devices listed for Monox, Inc. include WATCHCHILD.