510(k) K862182 ยท KXO Monitor, Pressure, Intrauterine
AMNIOINFUSION CATHETER
| Applicant | Michael Reese Hospital and Medical Center, Chicago IL, US |
| Decision | Substantially Equivalent, Aug 25, 1986 |
| Received | Jun 9, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K862182
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.