510(k) K000327 ยท HKO Refractometer, Ophthalmic
WAVESCAN WAVEFRONT SYSTEM MODEL HS 1
| Applicant | Visx, Incorporated, Santa Ana CA, US |
| Decision | Unknown, May 2, 2000 |
| Received | Feb 2, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000327
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.