| K-number | K170239 |
| Device name | Leica FL560 |
| Applicant | Leica Microsystems (Schweiz) AG |
| Product code | IZI |
| Device class | Class II |
| Decision date | Jul 5, 2017 |
| Decision | Substantially Equivalent — Kit Device |
| 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