ClearanceBrief
510(k) K111494 ยท DQA Oximeter

HANDHELD PULSE OXIMETER

ApplicantBeijing Choice Electronic Technololgy Co., Ltd., Shijingshan District, Beijing, CN
DecisionSubstantially Equivalent, Jan 18, 2012
ReceivedMay 31, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K111494

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.