ClearanceBrief
510(k) K810683 ยท FKX System, Peritoneal, Automatic Delivery

CAPD CATHETER ADAPTER

ApplicantAmerican Mcgaw, Mchenry IL, US
DecisionSubstantially Equivalent, May 8, 1981
ReceivedMar 13, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810683

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.