510(k) K093268 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
INTELLIVUE PATIENT MONITOR
| Applicant | Philips Medizinsysteme Boeblingen GmbH, Cardiac AN, Boeblingen, Baden-Wuerttemberg, DE |
| Decision | Substantially Equivalent, May 11, 2010 |
| Received | Oct 19, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093268
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 10, 2010 | Philips Healthcare Inc. Philips Intellivue Patient Monitor Model MP60 (M8005A) Terminated |
MHX | None listed |
| Aug 10, 2010 | Philips Healthcare Inc. Philips Intellivue Patient Monitor Model MP70 (M8007A) Terminated |
MHX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.