510(k) K040969 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
POISE DATAENGINE
| Applicant | Poise Technology Corporation, Hsin Chu City, TW |
| Decision | Substantially Equivalent, Jun 8, 2004 |
| Received | Apr 14, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040969
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.