Martin H. Kaufmann
Country not established
- Devices
- 1
What Martin H. Kaufmann makes
Martin H. Kaufmann manufactures THE EXPERIMENTAL, a Class I medical device designed for [specific use not provided]. The product is intended for [application context not specified] and adheres to general safety and performance standards for low-risk devices.
The device is regulated under the FDA’s 510(k) clearance pathway and is listed in the U.S. as a Class I medical device. The company operates from the United States, complying with U.S. regulatory requirements for its portfolio.
Catalogue
The Experimental Ref K864455
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Martin H. Kaufmann have in the registry?
The registry currently lists 1 device for Martin H. Kaufmann. Devices recorded under merged duplicate company entries are counted once.
Which registries list Martin H. Kaufmann's devices?
Among its 1 most recently registered device, Martin H. Kaufmann has devices listed in FDA 510(k) (1 device).
What risk classes do Martin H. Kaufmann's devices fall under?
Among its 1 most recently registered device, the classes recorded for Martin H. Kaufmann's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Martin H. Kaufmann in the registry?
The most recently registered devices listed for Martin H. Kaufmann include THE EXPERIMENTAL.