510(k) K124038 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
BEDSIDE PAEDIATRIC EARLY WARNING SYSTEM (BEDSIDEPEWS)
| Applicant | Bedside Clinical Systems, Inc., Austin TX, US |
| Decision | Substantially Equivalent, Jun 21, 2013 |
| Received | Dec 28, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K124038
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.