510(k) K112877 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
COMEN MULTI-PARAMETER PATIENT MONITOR
| Applicant | Goldway (Us), Inc., San Marino CA, US |
| Decision | Substantially Equivalent, Nov 7, 2012 |
| Received | Sep 30, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112877
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.