510(k) K965185 ยท KYB Lens, Guide, Intraocular
ACRYPAK FOLDER
| Applicant | Alcon Laboratories, Fort Worth TX, US |
| Decision | Substantially Equivalent, Mar 31, 1997 |
| Received | Dec 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K965185
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.