Medical Device Manufacturer · US , St. Paul , MN

Ototronix, LLC - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2013
2
Total
2
Cleared
0
Denied

Ototronix, LLC has 2 FDA 510(k) cleared medical devices. Based in St. Paul, US.

Historical record: 2 cleared submissions from 2013 to 2014. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Ototronix, LLC Filter by specialty or product code using the sidebar.

2 devices
1–2 of 2
Filters
Filter by Specialty
All2 Neurology 1 Ear, Nose, Throat 1