ClearanceBrief
510(k) K964041 ยท KOC Accessories, Blood Circuit, Hemodialysis

CUTANEOUS COMPRESSION DEVICE FOR USE IN HEMODIALYSIS

ApplicantRobert R. Stevens, Miami Lakes FL, US
DecisionSubstantially Equivalent, Jan 30, 1997
ReceivedOct 8, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964041

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.