510(k) K081576 ยท DRF Catheter, Electrode Recording, Or Probe, Electrode Recording
BLAZER DX-20 DIAGNOSTIC CATHETER
| Applicant | Boston Scientific Corp, San Jose CA, US |
| Decision | Substantially Equivalent, Feb 3, 2009 |
| Received | Jun 5, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081576
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.