ClearanceBrief
510(k) K952293 ยท DSY Prosthesis, Vascular Graft, Of 6mm And Greater Diameter

VASCUTEK GELWEAVE VASCULAR GRAFT

ApplicantVascutek, Ltd., Austin TX, US
DecisionSubstantially Equivalent - Subject to Tracking Reg., Dec 19, 1995
ReceivedMay 16, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K952293

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.