510(k) K030931 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
C3 PATIENT MONITOR
| Applicant | Analogic Corp., Peabody MA, US |
| Decision | Substantially Equivalent, May 9, 2003 |
| Received | Mar 25, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K030931
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.