510(k) K161517 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Mortara Surveyor Patient Monitor
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jan 11, 2017 |
| Received | Jun 2, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161517
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.