American Laser Medical · Class II · Cleared Oct 21, 1997
| K-number | K972765 |
| Device name | NUVOLASE 720 SYSTEM FOR OPHTHALMOLOGY LASER |
| Applicant | American Laser Medical |
| Product code | GEX |
| Device class | Class II |
| Decision date | Oct 21, 1997 |
| Decision | Substantially Equivalent |
| Regulation | 878.4810 |
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