510(k) K071029 ยท DQX Wire, Guide, Catheter
CARDIODRIVE CATHETER ADVANCEMENT SYSTEM (CAS)
| Applicant | Stereotaxis, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Aug 24, 2007 |
| Received | Apr 11, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071029
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.