ClearanceBrief
510(k) K091564 ยท DQA Oximeter

NBM-200MP PULSE OXIMETRY DEVICE

ApplicantOrsense, Ltd., Kfar Saba, IL
DecisionSubstantially Equivalent, Mar 19, 2010
ReceivedMay 28, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K091564

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.