Nk-Optik America
Country not established
- Devices
- 1
What Nk-Optik America makes
Nk-Optik America manufactures the LC-250 Infrared Light Coagulator, a device used for retinal photocoagulation in ophthalmic procedures. This equipment emits infrared light to treat conditions such as diabetic retinopathy or retinal tears by sealing leaking blood vessels or damaged areas.
The LC-250 Infrared Light Coagulator is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) premarket notification process. The company is based in the United States.
Catalogue
Lc-250 Infrared Light Coagulator Ref K964380
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nk-Optik America have in the registry?
The registry currently lists 1 device for Nk-Optik America. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nk-Optik America's devices?
Among its 1 most recently registered device, Nk-Optik America has devices listed in FDA 510(k) (1 device).
What risk classes do Nk-Optik America's devices fall under?
Among its 1 most recently registered device, the classes recorded for Nk-Optik America's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nk-Optik America in the registry?
The most recently registered devices listed for Nk-Optik America include LC-250 INFRARED LIGHT COAGULATOR.