Cavitron Surgical Systems
Country not established
- Devices
- 1
What Cavitron Surgical Systems makes
Cavitron Surgical Systems manufactures the Cavitron Electrosurgical Module (CEM) and PAK, which are electrosurgical devices used in surgical procedures.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.
Catalogue
Cavitron Electrosurgical Module (Cem) And Pak Ref K881687
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cavitron Surgical Systems have in the registry?
The registry currently lists 1 device for Cavitron Surgical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cavitron Surgical Systems's devices?
Among its 1 most recently registered device, Cavitron Surgical Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Cavitron Surgical Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cavitron Surgical Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cavitron Surgical Systems in the registry?
The most recently registered devices listed for Cavitron Surgical Systems include CAVITRON ELECTROSURGICAL MODULE (CEM) AND PAK.