510(k) K130740 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
NIGHTINGALE MONITORING SYSTEM
| Applicant | Zoe Medical, Inc., Topsfield MA, US |
| Decision | Substantially Equivalent, Jul 23, 2013 |
| Received | Mar 19, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130740
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.