Light Age, Inc. · Class II · Cleared Sep 14, 2004
| K-number | K032991 |
| Device name | LIGHT AGE EPICARE ALEXANDRITE LASER, MODELS 501-1H, 501-SP, 501-LP AND 501-LPX |
| Applicant | Light Age, Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Sep 14, 2004 |
| 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