ClearanceBrief
510(k) K871209 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

NORFOLK MEDICAL NORPORT

ApplicantNorfolk Medical Products, Inc., Skokie IL, US
DecisionSubstantially Equivalent, Jun 24, 1987
ReceivedMar 25, 1987
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K871209

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.