510(k) K051374 ยท DQX Wire, Guide, Catheter
CARDIODRIVE CATHETER ADVANCEMENT SYSTEM
| Applicant | Stereotaxis, Inc., Saint Louis MO, US |
| Decision | Substantially Equivalent, Jun 23, 2005 |
| Received | May 26, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K051374
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.