510(k) K972200 ยท OYU Dna-Probe Kit, Human Chromosome
ANEUVYSION
| Applicant | Vysis, Downers Grove IL, US |
| Decision | Substantially Equivalent, Oct 20, 1997 |
| Received | Jun 10, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972200
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.