ClearanceBrief
510(k) K863559 ยท DQT Occluder, Catheter Tip

URESIL OCCLUSION BALLOON CATHETER

ApplicantUresil Corp., Skokie IL, US
DecisionSubstantially Equivalent, Oct 10, 1986
ReceivedSep 12, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863559

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.