Master Medical Services, Inc.
Country not established
- Devices
- 1
What Master Medical Services, Inc. makes
Master Medical Services, Inc. manufactures the Master I, a Class II medical device designed for [specific application not detailed in data]. This product is intended for [use context not provided in data].
The Master I is regulated under FDA 510(k) clearance as a Class II device and is listed in the U.S. regulatory system. The company is based in the United States.
Catalogue
Master I Ref K822696
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Master Medical Services, Inc. have in the registry?
The registry currently lists 1 device for Master Medical Services, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Master Medical Services, Inc.'s devices?
Among its 1 most recently registered device, Master Medical Services, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Master Medical Services, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Master Medical Services, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Master Medical Services, Inc. in the registry?
The most recently registered devices listed for Master Medical Services, Inc. include MASTER I.