Neurotronics, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Neurotronics, Inc. has 9 FDA 510(k) cleared medical devices. Based in Gainesville, US.
Last cleared in 2022. Active since 1997. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neurotronics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Neurotronics, Inc.
9 devices
Cleared
Jul 15, 2022
NomadAir PMU810
Neurology
133d
Cleared
Nov 16, 2018
Serenity Piezo Sensor, Serenity Thermocouple Sensor
Neurology
141d
Cleared
Jul 02, 2018
Serenity Body Position Sensor, Serenity RIP Sensors
Neurology
194d
Cleared
Jan 19, 2017
Polysmith Sleep System, Model NTI7593
Neurology
218d
Cleared
Feb 18, 2015
Polysmith Sleep System
Neurology
145d
Cleared
Aug 09, 2013
LIVE VIEW PANEL (LVP)
Neurology
85d
Cleared
Mar 18, 2010
NOMAD SLEEP SYSTEM RECORDER, MODEL PMU800
Neurology
197d
Cleared
May 09, 2007
POLYSMITH SLEEP SYSTEM, MODEL NTI5498
Neurology
223d
Cleared
Nov 12, 1997
NEUROTRONICS POLYSOMNOGRAPHY SYSTEM 101
Anesthesiology
184d