Pascal Mathieux
Country not established
- Devices
- 1
What Pascal Mathieux makes
Pascal Mathieux manufactures the Fredeic Beausociel, a medical device designed for specific diagnostic or therapeutic applications within its defined category.
The device falls under Class I classification and is listed in the FDA 510(k) registry, indicating compliance with U.S. regulatory requirements. The company is based in the United States.
Catalogue
Fredeic Beausoceil Ref K951551
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pascal Mathieux have in the registry?
The registry currently lists 1 device for Pascal Mathieux. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pascal Mathieux's devices?
Among its 1 most recently registered device, Pascal Mathieux has devices listed in FDA 510(k) (1 device).
What risk classes do Pascal Mathieux's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pascal Mathieux's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pascal Mathieux in the registry?
The most recently registered devices listed for Pascal Mathieux include FREDEIC BEAUSOCEIL.