ClearanceBrief
510(k) K112687 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

CONNEX(R) VITAL SIGNS MONITOR 6000 SERIES

ApplicantWelch Allyn, Inc., Skaneateles Falls NY, US
DecisionSubstantially Equivalent, Nov 22, 2011
ReceivedSep 15, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K112687

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.