Eclosion, Inc.
Country not established
- Devices
- 1
What Eclosion, Inc. makes
Eclosion, Inc. makes the ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM, a device used for electrophysiological feedback monitoring.
This device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Electro-Physio-Feedback-Xrroid* System Ref K892114
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Eclosion, Inc. have in the registry?
The registry currently lists 1 device for Eclosion, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Eclosion, Inc.'s devices?
Among its 1 most recently registered device, Eclosion, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Eclosion, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Eclosion, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Eclosion, Inc. in the registry?
The most recently registered devices listed for Eclosion, Inc. include ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM.