510(k) K101991 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
WEBSTER DUO-DECAPOLAR CATHETER
| Applicant | Biosense Webster, Inc., Diamond Bar CA, US |
| Decision | Substantially Equivalent, May 2, 2011 |
| Received | Jul 14, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101991
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.