510(k) K053522 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
PHILIPS MP40, MP50, MP60, MP70, MP80 AND MP90 INTELLIVUE PATIENT MONITORS, RELEASE D.00
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, Bw, DE |
| Decision | Substantially Equivalent, Jan 10, 2006 |
| Received | Dec 19, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K053522
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.