The Washington Group, Inc.
Country not established
- Devices
- 1
What The Washington Group, Inc. makes
The Washington Group, Inc. manufactures the URITROL-M, a medical device designed for urinary tract procedures.
The URITROL-M is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Uritrol-M Ref K842808
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Washington Group, Inc. have in the registry?
The registry currently lists 1 device for The Washington Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Washington Group, Inc.'s devices?
Among its 1 most recently registered device, The Washington Group, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do The Washington Group, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Washington Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Washington Group, Inc. in the registry?
The most recently registered devices listed for The Washington Group, Inc. include URITROL-M.