Lensar, Inc. · Class II · Cleared Mar 2, 2018
| K-number | K173346 |
| Device name | LENSAR Laser System - fs 3D (LLS-fs 3D) |
| Applicant | Lensar, Inc. |
| Product code | OOE |
| Device class | Class II |
| Decision date | Mar 2, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 886.4390 |
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