510(k) K150312 ยท DXX System, Catheter Control, Steerable
Vdrive system, Vdrive Duo, Vdrive with V-Sono
| Applicant | Stereotaxis, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Jun 17, 2015 |
| Received | Feb 9, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150312
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.