510(k) K041918 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
INTEGRATED PATIENT MONITORING SYSTEM
| Applicant | Invivo Research, Inc., Orlando FL, US |
| Decision | Substantially Equivalent, Oct 15, 2004 |
| Received | Jul 16, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041918
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.