ClearanceBrief
510(k) K203854 ยท DQA Oximeter

Pulse Oximeter

ApplicantShenzhen Hexin Zondan Medical Equipment Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Apr 23, 2021
ReceivedDec 31, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203854

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.