510(k) K061463 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
ESOPHAGEAL MAPPING CATHETER, MODEL D-1272-01-S
| Applicant | Biosense Webster, Inc., Diamond Bar CA, US |
| Decision | Substantially Equivalent, Aug 14, 2006 |
| Received | May 26, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061463
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.