510(k) K051373 ยท NDQ System, Catheter Or Guidewire, Steerable (Magnetic)
CRONUS GUIDEWIRE, MODEL 001-001470-1
| Applicant | Stereotaxis, Inc., Saint Louis MO, US |
| Decision | Substantially Equivalent, Dec 9, 2005 |
| Received | May 26, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K051373
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.