510(k) K072371 ยท DXX System, Catheter Control, Steerable
ODYSSEY WORKSTATION
| Applicant | Stereotaxis, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Nov 14, 2007 |
| Received | Aug 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072371
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.