Kingfisher Healthcare NV
United KingdomFDA applicant, unverified
- Devices
- 1
What Kingfisher Healthcare NV makes
Kingfisher Healthcare NV manufactures the KFH ENERGY (Model E1), a medical device designed for energy delivery in clinical settings, such as electrocautery or surgical applications.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II device and is listed in the U.S. regulatory registry. The manufacturer is based in the United States.
Catalogue
Kfh Energy, Model: E1 Ref K073008
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kingfisher Healthcare NV have in the registry?
The registry currently lists 1 device for Kingfisher Healthcare NV. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kingfisher Healthcare NV's devices?
Among its 1 most recently registered device, Kingfisher Healthcare NV has devices listed in FDA 510(k) (1 device).
What risk classes do Kingfisher Healthcare NV's devices fall under?
Among its 1 most recently registered device, the classes recorded for Kingfisher Healthcare NV's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kingfisher Healthcare NV in the registry?
The most recently registered devices listed for Kingfisher Healthcare NV include KFH ENERGY, MODEL: E1.