Oxyair Engineering, Inc.
Country not established
- Devices
- 1
What Oxyair Engineering, Inc. makes
Oxyair Engineering, Inc. manufactures the Model 3000A, a medical oxygen monitor designed to measure and display oxygen levels in clinical or patient care settings.
The company’s products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Monitor, Oxygen, Model 3000A Ref K781209
510(k) 510(k)
Frequently asked questions
How many devices does Oxyair Engineering, Inc. have in the registry?
The registry currently lists 1 device for Oxyair Engineering, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oxyair Engineering, Inc.'s devices?
Among its 1 most recently registered device, Oxyair Engineering, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Oxyair Engineering, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Oxyair Engineering, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oxyair Engineering, Inc. in the registry?
The most recently registered devices listed for Oxyair Engineering, Inc. include MONITOR, OXYGEN, MODEL 3000A.