ClearanceBrief
510(k) K151180 ยท IYE Accelerator, Linear, Medical

ScandiDos Delta4 Phantom+

ApplicantScandidos AB, Uppsala, SE
DecisionSubstantially Equivalent, Aug 19, 2015
ReceivedMay 4, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K151180

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.