510(k) K112303 ยท DQY Catheter, Percutaneous
RUBICON SUPPORT CATHETER
| Applicant | Boston Scientific, Maple Grove MN, US |
| Decision | Substantially Equivalent, Nov 9, 2011 |
| Received | Aug 11, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K112303
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.