510(k) K141015 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
INTELLIVUE PATIENT MONITOR MX400, INTELLIVUE PATIENT MONITOR MX450, INTELLIVUE PATIENT MONITOR MX500, INTELLIVUE PATIENT
| Applicant | Philips Medizinsysteme Boeblingen GmbH, Cardiac AN, Boeblingen, Baden-Wuerttemberg, DE |
| Decision | Substantially Equivalent, May 19, 2014 |
| Received | Apr 21, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K141015
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 26, 2016 | Philips Electronics North America Corporation IntelliVue Patient Monitor
Product Usage:
The monitors are indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. The monitor Terminated |
MHX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.