ClearanceBrief
510(k) K870187 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

NORFOLK NORPORT, SUBCUT. IMPLANTED DRUG DEL. DEPOT

ApplicantNorfolk Medical Products, Inc., Skokie IL, US
DecisionSubstantially Equivalent, May 7, 1987
ReceivedJan 16, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K870187

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.