510(k) K051897 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
TRIO MONITOR
| Applicant | Datascope Corp., Mahwh NJ, US |
| Decision | Substantially Equivalent, Aug 12, 2005 |
| Received | Jul 13, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K051897
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.