510(k) K050399 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
MRI COMPATIBLE PATIENT MONITORING SYSTEM, MODEL 3160
| Applicant | Invivo Research, Inc., Orlando FL, US |
| Decision | Substantially Equivalent, Aug 26, 2005 |
| Received | Feb 16, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050399
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.