Tivamed, Inc.
Country not established
- Devices
- 1
What Tivamed, Inc. makes
Tivamed, Inc. manufactures the TIVAMED COOLED RF SYSTEM, model 78001, which is a radiofrequency ablation device.
This device is classified as Class II and is listed in the FDA 510(k) registry, with the company based in the United States.
Catalogue
Tivamed Cooled Rf System, Model 78001 Ref K082962
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tivamed, Inc. have in the registry?
The registry currently lists 1 device for Tivamed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tivamed, Inc.'s devices?
Among its 1 most recently registered device, Tivamed, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Tivamed, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tivamed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tivamed, Inc. in the registry?
The most recently registered devices listed for Tivamed, Inc. include TIVAMED COOLED RF SYSTEM, MODEL 78001.