510(k) K953591 ยท OYU Dna-Probe Kit, Human Chromosome
CEP 8 SPECTRUMORANGE DNA PROBE KIT
| Applicant | Vysis, Downers Grove IL, US |
| Decision | Substantially Equivalent, Nov 29, 1996 |
| Received | Aug 1, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953591
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.