Ototronix, LLC is one of 5120 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ototronix, LLC - FDA 510(k) Cleared Devices
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: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Ototronix, LLC Filter by specialty or product code using the sidebar.
Ototronix, LLC — FDA 510(k) Products and Clearance History
2 devices
Cleared
Jun 19, 2014
PROCEM
Ear, Nose, Throat
98d
Cleared
Apr 26, 2013
NYSTAGRAM VIDEO NYSTAGMOGRAPHY SYSTEM
Neurology
88d