510(k) K190392 ยท GEX Powered Laser Surgical Instrument
WaveLight FS200 Patient Interface
| Applicant | Alcon Laboratories, Inc., Lake Forest CA, US |
| Decision | Substantially Equivalent, Mar 26, 2019 |
| Received | Feb 19, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K190392
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.