510(k) K060047 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
CARTO RMT EP NAVIGATION SYSTEM V8
| Applicant | Biosense Webster, Inc., Diamond Bar CA, US |
| Decision | Substantially Equivalent, Jun 19, 2006 |
| Received | Jan 6, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060047
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.