510(k) K061392 ยท JOY Device, Automated Cell-Locating
IKONISCOPE FASTFISH AUTO/AMNIOCYTE TEST SYSTEM
| Applicant | Ikonisys, Inc., New Haven CT, US |
| Decision | Substantially Equivalent, Aug 1, 2006 |
| Received | May 19, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061392
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.