510(k) K060541 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
THE PHILIPS MP20,MP30,MP40,MP50,MP60,MP70,MP80 AND MP90 INTELLIVUE ATIENT MONITORS
| Applicant | Philips Medizin Systeme Boblingen GmbH, Boblingen, DE |
| Decision | Substantially Equivalent, Mar 24, 2006 |
| Received | Mar 1, 2006 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K060541
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Aug 24, 2010 | Philips Healthcare Inc. Philips M1013A IntelliVue G1 Anesthesia Gas Modules with manifolds Terminated |
BSZ | None listed |
| Aug 24, 2010 | Philips Healthcare Inc. Philips M1019A IntelliVue G5 Anesthesia Gas Modules with manifolds Terminated |
BSZ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.