A.S.M.O.T.
Country not established
- Devices
- 1
What A.S.M.O.T. makes
A.S.M.O.T. manufactures cryosurgical equipment designed for controlled tissue destruction through freezing. These devices are intended for procedures such as skin lesion removal, tumor ablation, and other cryotherapy applications in clinical and cosmetic settings.
The company’s cryosurgical equipment is classified as Class II under FDA regulations and is authorised via the 510(k) pathway. The portfolio is listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.
Catalogue
Cryosurgical Equipment Ref K771320
510(k) 510(k)
Frequently asked questions
How many devices does A.S.M.O.T. have in the registry?
The registry currently lists 1 device for A.S.M.O.T.. Devices recorded under merged duplicate company entries are counted once.
Which registries list A.S.M.O.T.'s devices?
Among its 1 most recently registered device, A.S.M.O.T. has devices listed in FDA 510(k) (1 device).
What risk classes do A.S.M.O.T.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for A.S.M.O.T.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from A.S.M.O.T. in the registry?
The most recently registered devices listed for A.S.M.O.T. include CRYOSURGICAL EQUIPMENT.