510(k) K123002 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
VITAL SYNC SYSTEM
| Applicant | Covidien, Formerly Nellcor Puritan Bennett, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Feb 27, 2013 |
| Received | Sep 27, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123002
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.