510(k) K920044 ยท KXO Monitor, Pressure, Intrauterine
DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KIT
| Applicant | Telos Medical Corp., Keene CA, US |
| Decision | Substantially Equivalent, Apr 3, 1992 |
| Received | Jan 6, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K920044
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.