ClearanceBrief
510(k) K894100 ยท DQA Oximeter

OXYTRAK(TM) PULSE OXIMETER

ApplicantCritikon Company, LLC, Tampa FL, US
DecisionSubstantially Equivalent, May 9, 1990
ReceivedJun 9, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894100

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.