Microsulis Americas, Inc.
Country not established
- Devices
- 1
What Microsulis Americas, Inc. makes
Microsulis Americas, Inc. makes the Microsulis Tissue Ablation System, a device used for tissue ablation procedures.
The Microsulis Tissue Ablation System is classified as a Class II medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Microsulis Tissue Ablation System Ref K052919
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Microsulis Americas, Inc. have in the registry?
The registry currently lists 1 device for Microsulis Americas, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Microsulis Americas, Inc.'s devices?
Among its 1 most recently registered device, Microsulis Americas, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Microsulis Americas, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Microsulis Americas, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Microsulis Americas, Inc. in the registry?
The most recently registered devices listed for Microsulis Americas, Inc. include MICROSULIS TISSUE ABLATION SYSTEM.