510(k) K854244 ยท HLI Ophthalmoscope, Ac-Powered
THE KEELER ALL PUPIL INDIRECT OPHTHALMOSCOPE
| Applicant | Keeler Instruments, Inc., Broomall PA, US |
| Decision | Substantially Equivalent, Nov 12, 1985 |
| Received | Oct 21, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K854244
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| May 22, 2008 | Keeler Instruments Inc Keeler All Pupil II Indirect Ophthalmoscope, Keeler Instruments, Inc., Broomall, PA 19008 Terminated |
HLI | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.