510(k) K061602 ยท JOY Device, Automated Cell-Locating
DUET SYSTEM
| Applicant | Bioview , Ltd., Tel Aviv, IL |
| Decision | Substantially Equivalent, Jan 23, 2007 |
| Received | Jun 8, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061602
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.