ClearanceBrief
510(k) K090599 ยท DQA Oximeter

MD300K1 PULSE OXIMETER

ApplicantBeijing Choice Electronic Technololgy Co., Ltd., Shijingshan District, Beijing, CN
DecisionSubstantially Equivalent, Jul 20, 2009
ReceivedMar 5, 2009
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K090599

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.