510(k) K862517 ยท HLF Device, Measuring, Lens Radius, Ophthalmic
BAUSCH & LOMB CONTACT LENS VIEWER
| Applicant | Bausch & Lomb, Inc., Rochester NY, US |
| Decision | Substantially Equivalent, Aug 11, 1986 |
| Received | Jul 1, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862517
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.