510(k) K023249 ยท NCF Aberrometer, Ophthalmic
ALCON LADARWAVE CUSTOMCORNEA WAVEFRONT SYSTEM
| Applicant | Alcon Laboratories, Inc., Orlando FL, US |
| Decision | Substantially Equivalent, Oct 18, 2002 |
| Received | Sep 30, 2002 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K023249
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 6, 2003 | Alcon Laboratories, Inc. ''Alcon Ladarwave CustomCornea Wavefront System'' Aberrometer software Version 7.91 Terminated |
None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.