ClearanceBrief
510(k) K061713 ยท IYE Accelerator, Linear, Medical

MAGIS1;MAGIS2

ApplicantDirex Systems Corp., Canton MA, US
DecisionSubstantially Equivalent, Jul 21, 2006
ReceivedJun 19, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K061713

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.