ClearanceBrief
510(k) K193243 ยท IYE Accelerator, Linear, Medical

Alta Multipurpose Device

ApplicantQfix, Avondale PA, US
DecisionSubstantially Equivalent, Feb 28, 2020
ReceivedNov 25, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K193243

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.