510(k) K922323 ยท KXO Monitor, Pressure, Intrauterine
MX4042/MC4044 SERIES SIMULCATH(TM)
| Applicant | Medex, Inc., Hilliard OH, US |
| Decision | Substantially Equivalent, Jun 14, 1994 |
| Received | May 4, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922323
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.