510(k) K132359 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
MRI PATIENT MONITORING SYSTEM
| Applicant | Invivo Corporation, Orlando FL, US |
| Decision | Substantially Equivalent, Aug 30, 2013 |
| Received | Jul 30, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K132359
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.