F.I.T. of France
Country not established
- Devices
- 1
What F.I.T. of France makes
F.I.T. of France manufactures the Biovision Emerald Laser Photocoagulator, a device used for retinal photocoagulation procedures to treat conditions such as diabetic retinopathy and macular edema by applying precise laser energy to the retina.
The Biovision Emerald Laser Photocoagulator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Biovision Emerald Laser Photocoagulator Ref K895363
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does F.I.T. of France have in the registry?
The registry currently lists 1 device for F.I.T. of France. Devices recorded under merged duplicate company entries are counted once.
Which registries list F.I.T. of France's devices?
Among its 1 most recently registered device, F.I.T. of France has devices listed in FDA 510(k) (1 device).
What risk classes do F.I.T. of France's devices fall under?
Among its 1 most recently registered device, the classes recorded for F.I.T. of France's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from F.I.T. of France in the registry?
The most recently registered devices listed for F.I.T. of France include BIOVISION EMERALD LASER PHOTOCOAGULATOR.