FDA 510(k) Applications Submitted by NEUROVIRTUAL USA, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K191095 |
04/25/2019 |
Maxxi Snore Sensor |
Neurovirtual USA, INC. |
| K171304 |
05/03/2017 |
Maxxi Rip Sensor |
Neurovirtual USA, INC. |
| K131335 |
05/09/2013 |
BWMINI EEG, BWMINIHST, BWMINI PSG |
NEUROVIRTUAL USA, INC. |
| K191492 |
06/05/2019 |
Maxxi Position Sensor |
Neurovirtual USA, INC. |
| K201495 |
06/05/2020 |
Maxxi Flow Sensor |
Neurovirtual USA, INC. |
| K112107 |
07/22/2011 |
BWIII EEG, BWIII EEG PLUS, BWIII PSG, BWIII PSG PLUS |
NEUROVIRTUAL USA, INC. |
| K062533 |
08/29/2006 |
BWII EEG DIGITAL, MODEL PV 1652; BWII PSG DIGITAL, MODEL PV 1524 |
NEUROVIRTUAL USA, INC. |
| K163547 |
12/16/2016 |
MaxxiGold Electrode 48, MaxxiGold Electrode 60, MaxxiGold Electrode 96 |
NEUROVIRTUAL USA, INC. |
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