ClearanceBrief
510(k) K920036 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

SURECATH PORT ACCESS CATHETER

ApplicantIvion Corp., Broomfield CO, US
DecisionSubstantially Equivalent, Nov 25, 1992
ReceivedJan 6, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K920036

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.