510(k) K830019 ยท HIO Sampler, Amniotic Fluid (Amniocentesis Tray)
AMNIO CENTESES KIT W/NEEDLE
| Applicant | Universal Medical Instrument Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 18, 1983 |
| Received | Jan 4, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830019
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.