510(k) K885316 ยท KXO Monitor, Pressure, Intrauterine
DISPOSABLE INTRAUTERINE PRESSURE KIT MODEL 13972A
| Applicant | Hewlett-Packard Co., Andover MA, US |
| Decision | Substantially Equivalent, Mar 23, 1989 |
| Received | Dec 29, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885316
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.