510(k) K043457 ยท DQX Wire, Guide, Catheter
MODIFICATION TO ENDOVASCULAR GUIDE WIRE
| Applicant | Stereotaxis, Inc., Saint Louis MO, US |
| Decision | Substantially Equivalent, Feb 28, 2005 |
| Received | Dec 15, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K043457
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.