510(k) K021802 ยท DQY Catheter, Percutaneous
STEREOTAXIS CATHETER ADVANCER SYSTEM
| Applicant | Stereotaxis, Inc., Saint Louis MO, US |
| Decision | Substantially Equivalent, Apr 8, 2003 |
| Received | Jun 3, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021802
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.