510(k) K970029 ยท HLJ Ophthalmoscope, Battery-Powered
KEELER SPECTRA INDIRECT OPHTHALMOSCOPE
| Applicant | Keeler Instruments, Inc., Broomall PA, US |
| Decision | Substantially Equivalent, Apr 2, 1997 |
| Received | Jan 3, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970029
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.