510(k) K042850 ยท DQY Catheter, Percutaneous
CARDIODRIVE, MODEL 001-004115 (NON-STERILE); 001-1169-1 (STERILE)
| Applicant | Stereotaxis, Inc., Saint Louis MO, US |
| Decision | Substantially Equivalent, Aug 9, 2006 |
| Received | Oct 15, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K042850
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.