ClearanceBrief
510(k) K912880 ยท DQA Oximeter

VITALMAX 510/520

ApplicantPace Tech, Inc., Clearwater FL, US
DecisionSubstantially Equivalent, Nov 14, 1991
ReceivedJul 1, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K912880

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.