ClearanceBrief
510(k) K863723 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

NORFOLK NORPORT/SUBCUTAN. IMPLANTED DRUG DEPOT

ApplicantNorfolk Medical Products, Inc., Skokie IL, US
DecisionSubstantially Equivalent, Oct 29, 1986
ReceivedSep 23, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K863723

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.