Electro Optical Instruments
Country not established
- Devices
- 1
What Electro Optical Instruments makes
Electro Optical Instruments manufactures systems for generating retinal reflex imagery, used primarily in ophthalmic diagnostics to capture detailed visualizations of the retina.
The company’s portfolio is regulated under FDA Class I devices, with relevant products listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Generated Retinal Reflex Imagery Sys Ref K840840
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Electro Optical Instruments have in the registry?
The registry currently lists 1 device for Electro Optical Instruments. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electro Optical Instruments's devices?
Among its 1 most recently registered device, Electro Optical Instruments has devices listed in FDA 510(k) (1 device).
What risk classes do Electro Optical Instruments's devices fall under?
Among its 1 most recently registered device, the classes recorded for Electro Optical Instruments's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Electro Optical Instruments in the registry?
The most recently registered devices listed for Electro Optical Instruments include GENERATED RETINAL REFLEX IMAGERY SYS.