General Project
Country not established
- Devices
- 1
What General Project makes
General Project manufactures the MD 30 COMPACT, a Class II medical device designed for [specific application not provided in data].
The MD 30 COMPACT is regulated under the FDA’s 510(k) pathway and is listed in the US. The company is based in the United States.
Catalogue
Md 30 Compact Ref K004014
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does General Project have in the registry?
The registry currently lists 1 device for General Project. Devices recorded under merged duplicate company entries are counted once.
Which registries list General Project's devices?
Among its 1 most recently registered device, General Project has devices listed in FDA 510(k) (1 device).
What risk classes do General Project's devices fall under?
Among its 1 most recently registered device, the classes recorded for General Project's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from General Project in the registry?
The most recently registered devices listed for General Project include MD 30 COMPACT.