FDA 510(k) Applications Submitted by Neurotronics, Inc.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K131415 |
05/16/2013 |
LIVE VIEW PANEL (LVP) |
NEUROTRONICS, INC. |
K161650 |
06/15/2016 |
Polysmith Sleep System, Model NTI7593 |
Neurotronics, Inc. |
K181709 |
06/28/2018 |
Serenity Piezo Sensor, Serenity Thermocouple Sensor |
Neurotronics, Inc. |
K142774 |
09/26/2014 |
Polysmith Sleep System |
Neurotronics, Inc. |
K173868 |
12/20/2017 |
Serenity Body Position Sensor, Serenity RIP Sensors |
Neurotronics, Inc. |
K971803 |
05/12/1997 |
NEUROTRONICS POLYSOMNOGRAPHY SYSTEM 101 |
NEUROTRONICS, INC. |
K092699 |
09/02/2009 |
NOMAD SLEEP SYSTEM RECORDER, MODEL PMU800 |
NEUROTRONICS, INC. |
K220631 |
03/04/2022 |
NomadAir PMU810 |
Neurotronics, Inc. |
K062943 |
09/28/2006 |
POLYSMITH SLEEP SYSTEM, MODEL NTI5498 |
NEUROTRONICS, INC. |
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