510(k) K961242 ยท KYB Lens, Guide, Intraocular
AMO PHACOFLEX II INTERSECTION SYSTEM
| Applicant | Allergan, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Jun 17, 1996 |
| Received | Apr 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K961242
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.