ClearanceBrief
510(k) K881690 ยท LKG Port & Catheter, Implanted, Subcutaneous, Intraventricular

PORT-A-CATH PORTAL INTRODUCER FORCEPS

ApplicantPharmacia Deltec, Inc., St. Paul MN, US
DecisionSubstantially Equivalent, May 20, 1988
ReceivedApr 19, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K881690

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.