Intra Lase Corp.
FDA 510(k) & PMA Approved Devices — 9 products
Advertisement
Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K073404 | IFS LASER SYSTEM | GEX | 2008-04-25 | View |
| 510(k) | K063682 | INTRALASE FUSION LASER | GEX | 2007-02-09 | View |
| 510(k) | K060372 | INTRALASE FS LASER, INTRALASE FS30 LASER, MODELS 1, 2, 3 | GEX | 2006-08-16 | View |
| 510(k) | K041893 | INTRALASE FS LASER | GEX | 2005-07-29 | View |
| 510(k) | K031960 | INTRALASE FS LASER | GEX | 2003-09-29 | View |
| 510(k) | K013941 | PULSION FS LASER KERATOME | GEX | 2002-02-27 | View |
| 510(k) | K002890 | INTRALASE 600C LASER KERATOME | GEX | 2001-08-09 | View |
| 510(k) | K001211 | MODIFICATION TO INTRALASE 600C LASER KERATOME | GEX | 2000-12-04 | View |
| 510(k) | K993153 | INTRALASE 600C LASER KERATOME | GEX | 1999-12-17 | View |
No matching devices.
Advertisement