510(k) K063694 ยท KYB Lens, Guide, Intraocular
AKREOS SINGLE USE INSERTION DEVICE, MODEL AI-28
| Applicant | Bausch & Lomb, Inc., San Dimas CA, US |
| Decision | Substantially Equivalent, Mar 7, 2007 |
| Received | Dec 13, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K063694
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.