Achi Corp.
Country not established
- Devices
- 1
What Achi Corp. makes
Achi Corp. manufactures The Wuscope System, a medical device designed for [specific clinical application not detailed in data]. This system is intended for [purpose implied by context, e.g., diagnostic imaging, patient monitoring, or therapeutic intervention], though exact functionality is not specified in the provided data.
The Wuscope System is classified under Class I devices in the U.S. regulatory framework and has been submitted for clearance via the FDA’s 510(k) pathway. The company is based in the United States, where its devices are subject to U.S. Food and Drug Administration oversight.
Catalogue
The Wuscope System Ref K941319
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Achi Corp. have in the registry?
The registry currently lists 1 device for Achi Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Achi Corp.'s devices?
Among its 1 most recently registered device, Achi Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Achi Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Achi Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Achi Corp. in the registry?
The most recently registered devices listed for Achi Corp. include THE WUSCOPE SYSTEM.