ClearanceBrief
510(k) K861165 ยท DQY Catheter, Percutaneous

PHARMASEAL DUAL LUMEN CATHETER

ApplicantAmerican Pharmaseal Div. Ahsc, Valencia CA, US
DecisionSubstantially Equivalent, May 5, 1986
ReceivedMar 28, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861165

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.