510(k) K981571 ยท KYB Lens, Guide, Intraocular
MONARCH IOL DELIVERY SYSTEM
| Applicant | Alcon Laboratories, Fort Worth TX, US |
| Decision | Substantially Equivalent, Jul 9, 1998 |
| Received | May 4, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981571
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.