ClearanceBrief
510(k) K820110 ยท DQA Oximeter

BIOX III

ApplicantBiox Technology, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 12, 1982
ReceivedJan 15, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820110

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.