510(k) K121013 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)
CONNEX VITAL SIGNS MONITOR 6000 SERIES
| Applicant | Welch Allyn, Inc., Skaneateles Falls NY, US |
| Decision | Substantially Equivalent, Jul 26, 2012 |
| Received | Apr 3, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121013
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.