510(k) K131913 ยท DRG Transmitters And Receivers, Physiological Signal, Radiofrequency
INTELLIVUE CL SPO2 POD AND CL NBP POD, PHILIPS INTELLIVUE PATIENT MONITORS MP5, MP5T, MP5SC
| Applicant | Philips Medizin Systeme Boeblingen GmbH, Boeblingen, Bw, DE |
| Decision | Substantially Equivalent, Nov 26, 2013 |
| Received | Jun 26, 2013 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K131913
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 21, 2014 | Philips Medical Systems, Inc. Philips IntelliVue Monitors with software revisions J.21.03, J.21.19.
Model Product
MP5 M8105A;
MP5SC M8105AS;
MP5T M8105AT;
MP5 Upgrade M8105AU ;
MP5SC Upgrade 866327
The monitors are intend Terminated |
MHX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.