510(k) K132038 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
ACCUTORR 7 VITAL SIGNS MONITOR
| Applicant | Mindray North America, Mahwh NJ, US |
| Decision | Substantially Equivalent, May 2, 2014 |
| Received | Jul 1, 2013 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K132038
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.