510(k) K122659 · DQX Wire, Guide, Catheter

VDRIVE W/V-SONO

Applicant	Stereotaxis, Inc., St. Louis MO, US
Decision	Substantially Equivalent, Jul 26, 2013
Received	Aug 31, 2012
Type	Traditional
FDA record	Open on fda.gov

Recalls that name K122659

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.