ClearanceBrief
510(k) K964881 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

ULTRAVERSE PTA CATHETER

ApplicantVas-Cath, Inc., Mississauga, Ontario, CA
DecisionSubstantially Equivalent, May 28, 1997
ReceivedDec 5, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964881

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.