510(k) K014261 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
ST/AR ST AND ARRHYTHMIA SOFTWARE, MODEL RELEASE E.0
| Applicant | Philips Medical Systems, Inc., Andover MA, US |
| Decision | Substantially Equivalent, Feb 12, 2002 |
| Received | Dec 27, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K014261
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.