ClearanceBrief
510(k) K172792 ยท DQA Oximeter

Handheld Pulse Oximeter, Model SP-20

ApplicantShenzhen Creative Industry Co., Ltd., Shenzhen, CN
DecisionSubstantially Equivalent, Nov 13, 2018
ReceivedSep 15, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K172792

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.