ClearanceBrief
510(k) K864552 ยท LLD Port & Catheter, Implanted, Subcutaneous, Intraperitoneal

PORT-A-CATH IMPLANTABLE CATHETER SYSTEM

ApplicantPharmacia, Inc., Piscataway NJ, US
DecisionSubstantially Equivalent, Mar 31, 1987
ReceivedNov 19, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K864552

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.