510(k) K900540 ยท DSI Detector And Alarm, Arrhythmia
TRAM PATIENT MONITOR
| Applicant | Marquette Electronics, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jul 17, 1990 |
| Received | Feb 5, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900540
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 22, 2014 | GE Healthcare, LLC GE Healthcare, TRAM MODULE, High-acuity patient monitoring. Product Usage: The TRAM Module is intended to provide uninterrupted monitoring of physiologic parameter data on adult, pediatric and neonata Terminated |
MHX | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.