ClearanceBrief
510(k) K120343 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

CONNEX WORKSTATION

ApplicantWelch Allyn, Inc., Skaneateles Falls NY, US
DecisionSubstantially Equivalent, Feb 24, 2012
ReceivedFeb 3, 2012
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K120343

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.