# Neurovirtual USA, Inc.

- Location (FDA's records): Doral, FL
- FDA decisions: 8 (2006–2020): 8 510(k) clearances
- Product codes: MNR (3), GWQ (3), OLT (1), GXY (1)
- 510(k) review time since 2016: median 266 days, against 192 for FDA's reviews in the same codes and years (0 of 5 faster)
- Predicates its devices cite: 17 (2 its own); citations of its devices by later devices: 2 (2 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Excel Tech., Ltd.: 4 (https://510kreport.com/company/excel-tech)
- Cadwell Laboratories, Inc.: 3 (https://510kreport.com/company/cadwell-laboratories)
- Epm Information Systems, Inc.: 2 (https://510kreport.com/company/epm-information-systems)
- Persyst Development Corporation: 1 (https://510kreport.com/company/persyst-development)
- Braebon Medical Corp.: 1 (https://510kreport.com/company/braebon-medical)
- Nox Medical Ehf: 1 (https://510kreport.com/company/nox-medical)
- Epm Development Systems Corp.: 1 (https://510kreport.com/company/epm-development-systems)
- The Electrode Store, Inc.: 1 (https://510kreport.com/company/electrode-store)

## Its most-cited devices
- K062533: Bwii Eeg Digital, Model PV 1652; Bwii PSG Digital, Model PV 1524 (2006), cited by 1
- K131335: Bwmini Eeg, Bwminihst, Bwmini PSG (2015), cited by 1

## Recent decisions
- K201495: Maxxi Flow Sensor (Dec 14, 2020)
- K191492: Maxxi Position Sensor (Apr 24, 2020)
- K191095: Maxxi Snore Sensor (Jan 16, 2020)
- K171304: Maxxi Rip Sensor (Jun 24, 2019)
- K163547: MaxxiGold Electrode 48, MaxxiGold Electrode 60, MaxxiGold Electrode 96 (Apr 11, 2017)
- K131335: Bwmini Eeg, Bwminihst, Bwmini PSG (Feb 3, 2015)
- K112107: Bwiii Eeg, Bwiii Eeg Plus, Bwiii PSG, Bwiii PSG Plus (Oct 28, 2011)
- K062533: Bwii Eeg Digital, Model PV 1652; Bwii PSG Digital, Model PV 1524 (Dec 22, 2006)

Source page: https://510kreport.com/company/neurovirtual-usa