510(k) K071164 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
LIFE+CEL BATTERY
| Applicant | Amco International Manufacturing & Design, Inc., Elizabeth CO, US |
| Decision | Substantially Equivalent, Dec 7, 2007 |
| Received | Apr 26, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071164
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.