510(k) K121031 ยท GEX Powered Laser Surgical Instrument
WAVELIGHT FS200 PATIENT INTERFACE 1505
| Applicant | Alcon Research, Ltd., Fort Worth TX, US |
| Decision | Substantially Equivalent, Jun 21, 2012 |
| Received | Apr 5, 2012 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K121031
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.