510(k) K862519 ยท HOS Projector, Ophthalmic
BAUSCH & LOMB ACCU-CHART 3 ACUITY PROJECTOR
| Applicant | Bausch & Lomb, Inc., Rochester NY, US |
| Decision | Substantially Equivalent, Jul 23, 1986 |
| Received | Jul 1, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862519
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.