510(k) K101619 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
WELCH ALLYN 1500 PATIENT MONITOR
| Applicant | Schiller AG, Baar, CH |
| Decision | Substantially Equivalent, Nov 12, 2010 |
| Received | Jun 9, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101619
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.