Covidien LP, Formerly Know AS Valleylab, A Divison
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Valleylab Microwave Ablation Generator Ref K072687
Regimes: 510(k) Registry: 510(k)Forcetriad Electrosurgical Generator Ref K110268
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Covidien Lp, Formerly Know AS Valleylab, A Divison have in the registry?
The registry currently lists 2 devices for Covidien Lp, Formerly Know AS Valleylab, A Divison. Devices recorded under merged duplicate company entries are counted once.
Which registries list Covidien Lp, Formerly Know AS Valleylab, A Divison's devices?
Among its 2 most recently registered devices, Covidien Lp, Formerly Know AS Valleylab, A Divison has devices listed in FDA 510(k) (2 devices).
What risk classes do Covidien Lp, Formerly Know AS Valleylab, A Divison's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Covidien Lp, Formerly Know AS Valleylab, A Divison's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Covidien Lp, Formerly Know AS Valleylab, A Divison in the registry?
The most recently registered devices listed for Covidien Lp, Formerly Know AS Valleylab, A Divison include VALLEYLAB MICROWAVE ABLATION GENERATOR and FORCETRIAD ELECTROSURGICAL GENERATOR.