510(k) K131929 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
SURVEYOR CENTRAL STATION
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Dec 3, 2013 |
| Received | Jun 27, 2013 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K131929
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.