Lucid, Inc. · Class II · Cleared Sep 17, 2008
| K-number | K080788 |
| Device name | VIVASCOPE SYSTEM, MODEL 1500, 3000 |
| Applicant | Lucid, Inc. |
| Product code | PSN |
| Device class | Class II |
| Decision date | Sep 17, 2008 |
| Decision | Substantially Equivalent |
| Regulation | 878.4580 |
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