510(k) K896122 ยท KXO Monitor, Pressure, Intrauterine
AMNICATHDL(TM) DT-IUPC2 DUAL LUMEN TRANS. TIPPED
| Applicant | Spectramed, Inc., Oxnard CA, US |
| Decision | Substantially Equivalent, Jan 19, 1990 |
| Received | Oct 24, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K896122
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.