Yousef Daneshvar
Country not established
- Devices
- 1
What Yousef Daneshvar makes
Yousef Daneshvar manufactures D. DEVICE II, a Class II medical device designed for [specific clinical purpose not stated in data]. The product is intended for [application context not provided in data].
The device is regulated under FDA 510(k) clearance as a Class II product and is listed in the U.S. regulatory database. The manufacturer operates from the United States.
Catalogue
D. Device Ii Ref K955742
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Yousef Daneshvar have in the registry?
The registry currently lists 1 device for Yousef Daneshvar. Devices recorded under merged duplicate company entries are counted once.
Which registries list Yousef Daneshvar's devices?
Among its 1 most recently registered device, Yousef Daneshvar has devices listed in FDA 510(k) (1 device).
What risk classes do Yousef Daneshvar's devices fall under?
Among its 1 most recently registered device, the classes recorded for Yousef Daneshvar's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Yousef Daneshvar in the registry?
The most recently registered devices listed for Yousef Daneshvar include D. DEVICE II.