510(k) K854197 ยท KYB Lens, Guide, Intraocular
IOSERT LENS IMPLANT INSTRUMENT
| Applicant | Chiron Vision Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 22, 1986 |
| Received | Oct 15, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854197
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.