| K-number | K112098 |
| Device name | TBD |
| Applicant | Lensar, Inc. |
| Product code | OOE |
| Device class | Class II |
| Decision date | Oct 19, 2011 |
| 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