Mivenion GmbH · Class II · Cleared Jan 31, 2014
| K-number | K130003 |
| Device name | XIRALITE FLOURESCENCE IMAGING SYSTEM X4 |
| Applicant | Mivenion GmbH |
| Product code | IZI |
| Device class | Class II |
| Decision date | Jan 31, 2014 |
| Decision | Substantially Equivalent |
| Regulation | 892.1600 |
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