ClearanceBrief
510(k) K101568 ยท DQA Oximeter

MODEL SB100II FINGER PULSE OXIMETER

ApplicantAtlantean, Bonita Springs FL, US
DecisionSubstantially Equivalent, Sep 20, 2010
ReceivedJun 2, 2010
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K101568

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.