ClearanceBrief
510(k) K223435 ยท QBJ Integrated Continuous Glucose Monitoring System, Factory Calibrated

FreeStyle Libre 3 Continuous Glucose Monitoring System; FreeStyle Libre 2 Flash Glucose Monitoring System

ApplicantAbbott Diabetes Care, Inc., Alameda CA, US
DecisionSubstantially Equivalent, Apr 13, 2023
ReceivedNov 14, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223435

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.