ClearanceBrief
510(k) K032937 ยท DXX System, Catheter Control, Steerable

NAVIGANT MAGNETIC NAVIGATION WORKSTATION 2.1 (NWS2) MODEL, 020-004500

ApplicantStereotaxis, Inc., Saint Louis MO, US
DecisionSubstantially Equivalent, Jul 1, 2004
ReceivedSep 22, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K032937

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.