ClearanceBrief
510(k) K223834 ยท IYE Accelerator, Linear, Medical

AccuCheck

ApplicantManteia Technologies Co., Ltd., Xiamen, CN
DecisionSubstantially Equivalent, Jul 20, 2023
ReceivedDec 22, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223834

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.