510(k) K123359 ยท FCW Light Source, Fiberoptic, Routine
OVS1 VIDEO SYSTEM
| Applicant | Olive Medical Corp., Salt Lake City UT, US |
| Decision | Substantially Equivalent, Dec 19, 2012 |
| Received | Oct 31, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123359
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.