510(k) K040776 ยท DQO Catheter, Intravascular, Diagnostic
ATLANTIS SR, MODEL C4020; ATLANTIS SR PLUS, MODEL 35975
| Applicant | Boston Scientific Corp, Fremont CA, US |
| Decision | Substantially Equivalent, Apr 29, 2004 |
| Received | Mar 26, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K040776
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.