510(k) K000731 ยท HLI Ophthalmoscope, Ac-Powered
MODIFICATION TO RTA RETINAL THICKNESS ANALYZER
| Applicant | Talia Technology , Ltd., Washington, D.C. DC, US |
| Decision | Substantially Equivalent, Mar 31, 2000 |
| Received | Mar 6, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K000731
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.