| K-number | K191693 |
| Device name | BC-5 |
| Applicant | Reveallux, Corp |
| Product code | GEX |
| Device class | Class II |
| Decision date | Nov 1, 2019 |
| Decision | Substantially Equivalent |
| Regulation | 878.4810 |
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