ClearanceBrief
510(k) K121806 ยท DQA Oximeter

BESIDE RESPIRATORY PATIENT MONITORING SYSTEM BESIDE RESIRATORY PATIENT MONITORING SYSTEM WITH RESPIRATION RATE SOFTWARE

ApplicantCovidien, Boulder CO, US
DecisionSubstantially Equivalent, Sep 28, 2012
ReceivedJun 20, 2012
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K121806

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.