510(k) K082887 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
PM-1000F+PATIENT MONITOR
| Applicant | Advanced Instrumentations, Inc., Hialeah FL, US |
| Decision | Substantially Equivalent, Jan 16, 2009 |
| Received | Sep 30, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082887
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.