ClearanceBrief
510(k) K062922 ยท KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

MODIFICATION TO AQUADEX FLEXFLOW SYSTEM

ApplicantChf Solutions, Inc., Brooklyn Park Mn MN, US
DecisionSubstantially Equivalent, Dec 13, 2006
ReceivedSep 28, 2006
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K062922

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.