510(k) K060221 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
THE PHILLIPS, MODEL MP20,MP30,MP40,MP50,MP60,MP70,MP80,AND MP90 INTELLIVUE PATIENT MONITORS
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, Baden-Wuerttemberg, DE |
| Decision | Substantially Equivalent, Feb 17, 2006 |
| Received | Jan 30, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060221
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.