ClearanceBrief
510(k) K122046 ยท DQA Oximeter

WRIST PULSE OXIMETER

ApplicantBeijing Choice Electronic Technololgy Co., Ltd., Beijing, CN
DecisionSubstantially Equivalent, Feb 4, 2013
ReceivedJul 12, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122046

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.