510(k) K881857 ยท KXO Monitor, Pressure, Intrauterine
AMNICATH(TM) MODEL DT-IUPC TRANS. TIPPED INTRAU.
| Applicant | Spectramed, Inc., Oxnard CA, US |
| Decision | Substantially Equivalent, Feb 1, 1989 |
| Received | May 3, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881857
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.