510(k) K980688 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
INTEGRITI PATIENT MONITOR
| Applicant | Alliance Instruments, Vancouver WA, US |
| Decision | Substantially Equivalent, Mar 16, 1999 |
| Received | Feb 23, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980688
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.