ClearanceBrief
510(k) K962127 ยท DQA Oximeter

OHMEDA 3800 PULSE OXIMETER

ApplicantOhmeda Medical, Madison WI, US
DecisionSubstantially Equivalent, Oct 10, 1996
ReceivedJun 3, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K962127

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.