510(k) K012435 ยท NGY Cannula, Trocar, Ophthalmic
ENTRY SITE ALIGNMENT SYSTEM MODEL # CX9626
| Applicant | Bausch & Lomb, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Oct 2, 2001 |
| Received | Jul 31, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012435
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.