ClearanceBrief
510(k) K981359 ยท DQY Catheter, Percutaneous

GT LEGGIERO

ApplicantTerumo Medical Corp., Elkton MD, US
DecisionSubstantially Equivalent, Jan 27, 1999
ReceivedApr 14, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981359

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.