510(k) K843039 ยท HMX Cannula, Ophthalmic
SITE ANTERIOR CAPSULOTOMER
| Applicant | Chiron Vision Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Nov 21, 1984 |
| Received | Aug 2, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K843039
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.