510(k) K000637 ยท NCF Aberrometer, Ophthalmic
CUSTOMCORNEA MEASUREMENT DEVICE (CCMD)
| Applicant | Alcon Laboratories, Inc., Orlando FL, US |
| Decision | Unknown, May 19, 2000 |
| Received | Feb 25, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000637
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.