ClearanceBrief
510(k) K072825 ยท DQA Oximeter

FINGERTIP PULSE OXIMETER, MODEL MD300I

ApplicantBeijing Choice Electronic Technololgy Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, Jan 14, 2008
ReceivedOct 2, 2007
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K072825

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.