ClearanceBrief
510(k) K022084 ยท DQA Oximeter

ATLAS MONITOR, MODELS 200,210,220

ApplicantWelch Allyn, Inc., Skaneateles Falls NY, US
DecisionSubstantially Equivalent, Sep 26, 2002
ReceivedJun 27, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K022084

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.