510(k) K131032 ยท MHX Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
PHILIPS SURESIGNS CENTRAL
| Applicant | Philips Medical Systems, Andover MA, US |
| Decision | Substantially Equivalent, Aug 12, 2013 |
| Received | Apr 12, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K131032
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.