Neurovirtual USA, Inc.
Neurovirtual USA, Inc. appears in FDA public data with 0 recalls, 8 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Dec 14, 2020.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| 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 |