ClearanceBrief
510(k) K132808 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

VITAL SIGNS MONITOR, CONNEX VITAL SIGNS MONITOR

ApplicantWelch Allyn, Inc., Skaneateles Falls NY, US
DecisionSubstantially Equivalent, Nov 20, 2013
ReceivedSep 11, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K132808

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.