510(k) K061052 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
THE PHILIPS INTELLIVUE PATIENT MONITORS, MODELS MP20,MP30,MP40,MP50,MP60,MP70,MP80,MP90
| Applicant | Philips Medical Systems North America, Inc., Boeblingen, DE |
| Decision | Substantially Equivalent, May 26, 2006 |
| Received | Apr 17, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K061052
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.