E S C Sharplan · Class II · Cleared May 5, 2000
| K-number | K001263 |
| Device name | SHARPLAN LASERS, INC. PULSED CTH:YAG HOLMIUM SURGICAL LASER, MODEL 2040 |
| Applicant | E S C Sharplan |
| Product code | GEX |
| Device class | Class II |
| Decision date | May 5, 2000 |
| 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