510(k) K021422 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
PHILIPS INFORMATION CENTER SOFTWARE REVISION D.02
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, May 15, 2002 |
| Received | May 3, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021422
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.