510(k) K142032 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
MRI PATIENT MONITORING SYSTEM TESLA M3
| Applicant | Mipm Mammendorfer Institut Fur Physik Und Medizin, The Hague, NL |
| Decision | Substantially Equivalent, May 7, 2015 |
| Received | Jul 25, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142032
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.