ClearanceBrief
510(k) K080255 ยท DQA Oximeter

NONIN MEDICAL, INC., MODEL 7500 DIGITAL PULSE OXIMETER

ApplicantNonin Medical, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, May 23, 2008
ReceivedJan 31, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K080255

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.