510(k) K050877 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
CORONARY SINUS DEFLECTABLE MAPPING CATHETER, 4 FR, 5 FR, 6 FR & 7 FR
| Applicant | Biosense Webster, Inc., Diamond Bar CA, US |
| Decision | Substantially Equivalent, Jun 24, 2005 |
| Received | Apr 6, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050877
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.