ClearanceBrief
510(k) K151363 ยท DXC Clamp, Vascular

Zephyr Vascular Compression Device

ApplicantAdvanced Vascular Dynamics, Milwaukie OR, US
DecisionSubstantially Equivalent, Jul 31, 2015
ReceivedMay 21, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K151363

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.