510(k) K131829 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
INTELLIVUE PATIENT MONITOR
| Applicant | Philips Medizinsysteme Boeblingen GmbH, Cardiac AN, Boeblingen, Baden-Wuerttemberg, DE |
| Decision | Substantially Equivalent, Aug 16, 2013 |
| Received | Jun 20, 2013 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K131829
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.