ClearanceBrief
510(k) K121697 ยท DQA Oximeter

FINGERTIP PULSE OXIMETER

ApplicantAndon Health Co, Ltd., Tianjin, CN
DecisionSubstantially Equivalent, Oct 15, 2012
ReceivedJun 7, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K121697

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.