ClearanceBrief
510(k) K101445 ยท MWI Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

VITAL SIGNS MONITOR-VSM 6000 SERIES

ApplicantWelch Allyn, Inc., Skaneateles Falls NY, US
DecisionSubstantially Equivalent, Jun 8, 2010
ReceivedMay 24, 2010
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K101445

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.