ClearanceBrief
510(k) K133396 ยท DQX Wire, Guide, Catheter

VDRIVE WITH V-SONO

ApplicantStereotaxis, Inc., St. Louis MO, US
DecisionSubstantially Equivalent, Feb 6, 2014
ReceivedNov 6, 2013
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K133396

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.