510(k) K062392 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
PHILIPS MP5 INTELLIVUE PATIENT MONITOR
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, Baden-Wuerttemberg, DE |
| Decision | Substantially Equivalent, Sep 6, 2006 |
| Received | Aug 16, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K062392
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.