Innotech USA, Inc. · Class II · Cleared Mar 2, 2004
| K-number | K033251 |
| Device name | THE FRIENDLYLIGHT ND: YAG LASERS |
| Applicant | Innotech USA, Inc. |
| Product code | GEX |
| Device class | Class II |
| Decision date | Mar 2, 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