510(k) K122394 ยท DQY Catheter, Percutaneous
RUBICON 18 SUPPORT CATHETER
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Aug 30, 2012 |
| Received | Aug 7, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K122394
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.