510(k) K101449 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
INTELLIVUE PATIENT MONITOR
| Applicant | Philips Medizinsysteme Boeblingen GmbH, Cardiac AN, Boeblingen, DE |
| Decision | Substantially Equivalent, Jun 18, 2010 |
| Received | May 24, 2010 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K101449
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.