ClearanceBrief
510(k) K122405 ยท DXC Clamp, Vascular

AIR-BAND RADIAL COMPRESSION DEVICE

ApplicantDatascope Corp., Cardiac Assist Division, Fairfield NJ, US
DecisionSubstantially Equivalent, Nov 9, 2012
ReceivedAug 7, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122405

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.