ClearanceBrief
510(k) K113865 ยท DQA Oximeter

PULTOL

ApplicantSharp Corporation, Richardson TX, US
DecisionSubstantially Equivalent, Mar 21, 2012
ReceivedDec 30, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113865

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.