510(k) K113657 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
INTELLIVUE PATIENT MONITOR
| Applicant | Philips Medizin Systeme Boblingen GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Mar 22, 2012 |
| Received | Dec 12, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K113657
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.