ClearanceBrief
510(k) K031740 ยท DQA Oximeter

VSM - VITAL SIGNS MONITOR, MODEL 53000 SERIES

ApplicantWelch Allyn Protocol, Inc., Beaverton OR, US
DecisionSubstantially Equivalent, Aug 26, 2003
ReceivedJun 4, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031740

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.