Oxytec Medical Corporation
Country not established
- Devices
- 1
What Oxytec Medical Corporation makes
Oxytec Medical Corporation manufactures the OXYTEC Model 900, a medical device designed for oxygen therapy delivery, including portable and stationary systems for clinical and home-use settings.
The company’s portfolio is regulated under FDA Class II devices, with the Model 900 authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.
Catalogue
Oxytec, Model 900 Ref K043615
510(k) 510(k)
Frequently asked questions
How many devices does Oxytec Medical Corporation have in the registry?
The registry currently lists 1 device for Oxytec Medical Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oxytec Medical Corporation's devices?
Among its 1 most recently registered device, Oxytec Medical Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Oxytec Medical Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Oxytec Medical Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oxytec Medical Corporation in the registry?
The most recently registered devices listed for Oxytec Medical Corporation include OXYTEC, MODEL 900.