FDA Product Code
FDA Product Code LXS — Clearance Directory
- Device Class
- Class II
- Assigned Panel
- Ophthalmic
- 21 CFR Citation
- 886.4392
510(k) Clearances — 6 records
| K-Number | Device Name | Applicant | Decision Date | Clearance Type | Summary |
|---|---|---|---|---|---|
| K023045 | MICRORUPTER V | Meridian AG | 2002-09-26 | Traditional | PDF ↗ |
| K901605 | PHOENIX LASER SYSTEMS OPHTHALMIC SURGICAL WORKSTA. | Phoenix Laser Systems, Inc. | 1990-12-13 | Traditional | PDF ↗ |
| K895864 | MICRORUPTOR III SYST, Q-SWITCHED ND:YAG LASER COMP | Lasag AG | 1989-12-29 | Traditional | PDF ↗ |
| K893987 | NIDEK MODEL YC-1200 | Nidek, Inc. | 1989-08-18 | Traditional | PDF ↗ |
| K892204 | NIDEK INC. MODELS YC-2000 & 3000 OPHTHALMIC LASERS | Nidek, Inc. | 1989-06-22 | Traditional | PDF ↗ |
| K892058 | ISL QC 2000 | Intelligent Surgical Lasers, Inc. | 1989-06-15 | Traditional | PDF ↗ |
Product code LXS · Class II · Ophthalmic. Data: openFDA.