Mentor Ophthalmics, Inc. · Class II · Cleared Jul 14, 1997
| K-number | K971538 |
| Device name | MENTOR GEMINI HEMOSTATIC ERASER |
| Applicant | Mentor Ophthalmics, Inc. |
| Product code | HQO |
| Device class | Class II |
| Decision date | Jul 14, 1997 |
| Decision | Substantially Equivalent |
| Regulation | 886.4115 |
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