Gomi Medical Instruments
Country not established
- Devices
- 1
What Gomi Medical Instruments makes
Gomi Medical Instruments manufactures a single-breath lung diffusion test device used in spirometry for assessing pulmonary function, specifically measuring gas exchange efficiency in the lungs.
The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) pathway. The devices are based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gomi Medical Instruments have in the registry?
The registry currently lists 1 device for Gomi Medical Instruments. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gomi Medical Instruments's devices?
Among its 1 most recently registered device, Gomi Medical Instruments has devices listed in FDA 510(k) (1 device).
What risk classes do Gomi Medical Instruments's devices fall under?
Among its 1 most recently registered device, the classes recorded for Gomi Medical Instruments's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Gomi Medical Instruments in the registry?
The most recently registered devices listed for Gomi Medical Instruments include SINGLE BREATH LUNG DIFFUS TEST DEVICE SPIROMETERY.