510(k) K032087 ยท HLJ Ophthalmoscope, Battery-Powered
KEELER WIDE ANGLE OPHTHALMOSCOPE MODEL 1130-P-5004
| Applicant | Keeler Instruments, Inc., Broomall PA, US |
| Decision | Substantially Equivalent, Nov 26, 2003 |
| Received | Jul 7, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032087
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.