510(k) K103737 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
OMNI II PATIENT MONITOR
| Applicant | Infinium Medical, Appollo Beach FL, US |
| Decision | Substantially Equivalent, Jun 2, 2011 |
| Received | Dec 22, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K103737
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.