ClearanceBrief
510(k) K110516 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

CONNEX VITAL SIGNS MONITOR 6000 SERIES

ApplicantWelch Allyn, Inc., Skaneateles Falls NY, US
DecisionSubstantially Equivalent, Jun 1, 2011
ReceivedFeb 23, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K110516

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.