510(k) K032858 ยท DSI Detector And Alarm, Arrhythmia
THE PHILIPS INTELLIVUE MP40, MP50, MP60, MP70,AND MP90 PATIENT MONITORS, RELEASE B.O.
| Applicant | Philips Medizin Systeme Boblingen GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Oct 10, 2003 |
| Received | Sep 12, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032858
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.