ClearanceBrief
510(k) K931304 ยท DQA Oximeter

OHMEDA HAND HELD OXIMETER

ApplicantOhmeda Medical, Louisville CO, US
DecisionSubstantially Equivalent, Sep 29, 1994
ReceivedMar 15, 1993
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K931304

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.