ClearanceBrief
510(k) K012333 ยท DPZ Oximeter, Ear

FLEXI-SITE SP02 EAR SENSOR

ApplicantEpic Medical Equipment Services, Inc., Plano TX, US
DecisionSubstantially Equivalent, Oct 17, 2001
ReceivedJul 24, 2001
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K012333

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.