510(k) K002920 ยท HKI Camera, Ophthalmic, Ac-Powered
MEGAVISION CPX, MEGAVISION FA, MODEL I AND II
| Applicant | Escalon Medical Corp., New Berlin WI, US |
| Decision | Substantially Equivalent, Dec 18, 2000 |
| Received | Sep 19, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002920
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.