510(k) K790678 ยท KXO Monitor, Pressure, Intrauterine
INTRAUTERINE CATHETER TIP
| Applicant | Sonicaid, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 11, 1979 |
| Received | Apr 9, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790678
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.