ClearanceBrief
510(k) K070371 ยท DQA Oximeter

FINGERTIP PULSE OXIMETER MD300C

ApplicantBeijing Choice Electronic Technololgy Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, Aug 13, 2007
ReceivedFeb 8, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070371

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.