ClearanceBrief
510(k) K021555 ยท DXX System, Catheter Control, Steerable

STEREOTAXIS NIOBE MAGNETIC NAVIGATION SYSTEM

ApplicantStereotaxis, Inc., Saint Louis MO, US
DecisionSubstantially Equivalent, Jan 15, 2003
ReceivedMay 13, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K021555

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.