ClearanceBrief
510(k) K141530 ยท DXX System, Catheter Control, Steerable

VDRIVE SYSTEM/ VDRIVE DUO/ VDRIVE WITH V-CAS

ApplicantStereotaxis, Inc., Fairfax VA, US
DecisionSubstantially Equivalent, Dec 18, 2014
ReceivedJun 9, 2014
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K141530

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.