Medical Device Systems, Inc.
Country not established
- Devices
- 1
What Medical Device Systems, Inc. makes
Medical Device Systems, Inc. manufactures THE ULTRA, a Class II medical device designed for [specific clinical purpose or function—if not provided, omit or clarify if generic].
THE ULTRA is regulated under 510(k) clearance by the U.S. FDA and is listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
The Ultra Ref K935755
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medical Device Systems, Inc. have in the registry?
The registry currently lists 1 device for Medical Device Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medical Device Systems, Inc.'s devices?
Among its 1 most recently registered device, Medical Device Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Medical Device Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Medical Device Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medical Device Systems, Inc. in the registry?
The most recently registered devices listed for Medical Device Systems, Inc. include THE ULTRA.