510(k) K050684 ยท DQO Catheter, Intravascular, Diagnostic
ATLANTIS PV
| Applicant | Boston Scientific Corp, Fremont CA, US |
| Decision | Substantially Equivalent, May 20, 2005 |
| Received | Mar 17, 2005 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K050684
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.