510(k) K010288 ยท OYU Dna-Probe Kit, Human Chromosome
ANEUVYSION MULITICOLOR DNA PROBE KIT
| Applicant | Vysis, Downers Grove IL, US |
| Decision | Substantially Equivalent, Apr 13, 2001 |
| Received | Jan 31, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010288
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.