ClearanceBrief
510(k) K052829 ยท DQA Oximeter

WRISTOX MODEL 3100 PULSE OXIMETER

ApplicantNonin Medical, Inc., Plymouth MN, US
DecisionSubstantially Equivalent, Nov 10, 2005
ReceivedOct 5, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K052829

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.