ClearanceBrief
510(k) K092620 ยท DQA Oximeter

MD300C318 FINGERTIP PULSE OXIMETER

ApplicantBeijing Choice Electronic Technololgy Co., Ltd., Shijingshan District, Beijing, CN
DecisionSubstantially Equivalent, Dec 4, 2009
ReceivedAug 26, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K092620

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.