ClearanceBrief
510(k) K201468 ยท DQA Oximeter

Pulse Oximeter

ApplicantShenzhen Creative Industry Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Jan 25, 2021
ReceivedJun 2, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K201468

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.