Brain Ultimate, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 4
Catalogue
QuickVision Ultimate rTMS Ref K261228
510(k) 510(k)Ultimate rTMS for OCD (M-series) Ref K243459
510(k) 510(k)Ultimate rTMS Ref K243460
510(k) 510(k)Ultimate rTMS; Yingchi rTMS Ref K230735
510(k) 510(k)
Frequently asked questions
How many devices does Brain Ultimate, Inc. have in the registry?
The registry currently lists 4 devices for Brain Ultimate, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brain Ultimate, Inc.'s devices?
Among its 4 most recently registered devices, Brain Ultimate, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Brain Ultimate, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Brain Ultimate, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Brain Ultimate, Inc. in the registry?
The most recently registered devices listed for Brain Ultimate, Inc. include QuickVision Ultimate rTMS, Ultimate rTMS for OCD (M-series), Ultimate rTMS and Ultimate rTMS; Yingchi rTMS.