510(k) K150975 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Philips IntelliVue MP2/MP5/MPSC Patient Monitors, Philips IntelliVue X1 and X2 multi-msrmt-modules for use with IntelliVue patient monitors
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, DE |
| Decision | Substantially Equivalent, Jun 25, 2015 |
| Received | Apr 13, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K150975
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 23, 2017 | Philips Electronics North America Corporation IntelliVue Multi Measurement Server, IntelliVue Multi Measurement Server SLCP, IntelliVue Multi Measurement Server X2, IntelliVue Patient Monitor Models MP2 and MP5
Product Usage:
Indicated for use Open, Classified |
MHX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.