510(k) K120631 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
PATIENT MONITOR
| Applicant | Advanced Instruments, Inc., Hialeah FL, US |
| Decision | Substantially Equivalent, May 25, 2012 |
| Received | Mar 1, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120631
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.