510(k) K952480 ยท HKI Camera, Ophthalmic, Ac-Powered
ORIMS DIGITAL ANGIOGRAPHY SYSTEM
| Applicant | Midwest Ophthalmic Instruments, Inc., Romeoville IL, US |
| Decision | Substantially Equivalent, Aug 25, 1995 |
| Received | May 30, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K952480
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.