Respirics, Inc.
Country not established
- Devices
- 1
What Respirics, Inc. makes
Respirics, Inc. manufactures the MD TURBO, a medical device designed for respiratory support, specifically targeting patients requiring non-invasive ventilation or high-flow oxygen therapy.
The MD TURBO is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Md Turbo Ref K051284
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Respirics, Inc. have in the registry?
The registry currently lists 1 device for Respirics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Respirics, Inc.'s devices?
Among its 1 most recently registered device, Respirics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Respirics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Respirics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Respirics, Inc. in the registry?
The most recently registered devices listed for Respirics, Inc. include MD TURBO.