ClearanceBrief
510(k) K031465 ยท DQA Oximeter

MODEL 2100 PULSE OXIMETER

ApplicantDolphin Medical, Inc., Tampa FL, US
DecisionSubstantially Equivalent, Oct 10, 2003
ReceivedMay 8, 2003
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K031465

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.