510(k) K120774 ยท DSI Detector And Alarm, Arrhythmia
ACUITY CENTRAL MONITORING STATION OR ACUITY CENTRAL MONITORING SYSTEM, MOBILE ACUITY LT, MOBILE ACUITY, MOBILE LT
| Applicant | Welch Allyn, Inc., Skaneateles Falls NY, US |
| Decision | Substantially Equivalent, Apr 10, 2012 |
| Received | Mar 14, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K120774
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.