ClearanceBrief
510(k) K880072 ยท LLD Port & Catheter, Implanted, Subcutaneous, Intraperitoneal

PORT-A-CATH IMPLANTABLE DRUG DELIVERY SYSTEM

ApplicantPharmacia Deltec, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, Mar 29, 1988
ReceivedJan 11, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880072

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.