510(k) K120173 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
PATIENT MONITOR
| Applicant | Edan Instruments, Inc., Shenzhen, CN |
| Decision | Substantially Equivalent, May 16, 2012 |
| Received | Jan 20, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K120173
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.