ClearanceBrief
510(k) K112804 ยท DQA Oximeter

FINGERTIP PULSE OXIMETER

ApplicantGuangdong Biolight Meditech Co., Ltd., Shanghai, CN
DecisionSubstantially Equivalent, Jan 27, 2012
ReceivedSep 27, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K112804

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.