510(k) K013484 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
TELSTAR MAGNETIC NAVIGATION SYSTEMS [MNS}, TELSTAR BI-PLANE DIGITAL IMAGING SYSTEM, NIOBE ELECTROPHYSIOLOGY MAPPING CATH
| Applicant | Stereotaxis, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, May 2, 2002 |
| Received | Oct 19, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013484
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.