Bowater Research, Inc.
Country not established
- Devices
- 1
What Bowater Research, Inc. makes
Bowater Research, Inc. manufactures the ULTRATONE 8+ and ULTRATONE 20, which are diagnostic ultrasound devices used for imaging soft tissues and organs.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Ultratone 8+ & 20 Ref K926410
510(k) 510(k)
Frequently asked questions
How many devices does Bowater Research, Inc. have in the registry?
The registry currently lists 1 device for Bowater Research, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bowater Research, Inc.'s devices?
Among its 1 most recently registered device, Bowater Research, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Bowater Research, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bowater Research, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bowater Research, Inc. in the registry?
The most recently registered devices listed for Bowater Research, Inc. include ULTRATONE 8+ & 20.