510(k) K140641 ยท DYB Introducer, Catheter
VESSIX GUIDE SHEATH 7F, 45 CM, RDC, VESSIX GUIDE SHEATH 7F, 45CM, LIMA
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Jul 3, 2014 |
| Received | Mar 12, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K140641
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.