ClearanceBrief
510(k) K081125 ยท DQA Oximeter

WRIST PULSE OXIMETER MD300W

ApplicantBeijing Choice Electronic Technololgy Co., Ltd., Beijing, CN
DecisionSubstantially Equivalent, Jul 2, 2008
ReceivedApr 21, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K081125

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.