510(k) K031481 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
THE PHILIPS INTELLIVUE MP60, MP70, AND MP90 PATIENT MONITORS, RELEASE A.20
| Applicant | Philips Medizin Systeme Boblingen GmbH, Boeblingen, Baden-Wuerttemberg, DE |
| Decision | Substantially Equivalent, May 29, 2003 |
| Received | May 12, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K031481
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.