| K-number | K191095 |
| Device name | Maxxi Snore Sensor |
| Applicant | Neurovirtual USA, Inc. |
| Product code | MNR |
| Device class | Class II |
| Decision date | Jan 16, 2020 |
| Decision | Substantially Equivalent |
| Regulation | 868.2375 |
AI extraction for this record is queued and will appear within 24 hours. View full FDA record →
View the full FDA submission: accessdata.fda.gov