ClearanceBrief
510(k) K203208 ยท DQA Oximeter

Guardian Angel Rx GA2000 Series Digital Vital Sign Monitoring System

ApplicantTaiwan Aulisa Medical Devices Technologies, Inc., Taipei, TW
DecisionSubstantially Equivalent, Jun 12, 2022
ReceivedOct 30, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203208

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.