Engineered Medical Technology, Inc.
Country not established
- Devices
- 1
What Engineered Medical Technology, Inc. makes
Engineered Medical Technology, Inc. manufactures the Oxygen Applied Symptom Improvement System (OASIS), which is a device designed for oxygen delivery and symptom management.
The company is based in the United States, and its product is classified as a Class II medical device listed within the FDA 510(k) regulatory registry.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Engineered Medical Technology, Inc. have in the registry?
The registry currently lists 1 device for Engineered Medical Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Engineered Medical Technology, Inc.'s devices?
Among its 1 most recently registered device, Engineered Medical Technology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Engineered Medical Technology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Engineered Medical Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Engineered Medical Technology, Inc. in the registry?
The most recently registered devices listed for Engineered Medical Technology, Inc. include OXYGEN APPLIED SYMPTOM IMPROVEMENT SYSTEM (OASIS).