Deepwell Dtx, Inc.
Country not established
- Devices
- 1
What Deepwell Dtx, Inc. makes
Deepwell Dtx, Inc. manufactures an A Breathing System (ABS), a device designed to assist or support patient respiration in clinical settings.
The company’s portfolio is regulated under FDA Class II devices and includes submissions via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
A Breathing System (ABS) Ref K233580
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Deepwell Dtx, Inc. have in the registry?
The registry currently lists 1 device for Deepwell Dtx, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Deepwell Dtx, Inc.'s devices?
Among its 1 most recently registered device, Deepwell Dtx, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Deepwell Dtx, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Deepwell Dtx, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Deepwell Dtx, Inc. in the registry?
The most recently registered devices listed for Deepwell Dtx, Inc. include A Breathing System (ABS).