ClearanceBrief
510(k) K100203 ยท DQA Oximeter

HANDHELD PULSE OXIMETER MODEL MD300A/ MD300K2/ MD300M

ApplicantBeijing Choice Electronic Technololgy Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, May 17, 2010
ReceivedJan 25, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K100203

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.