510(k) K152401 ยท DQY Catheter, Percutaneous
Stingray LP Catheter
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Dec 4, 2015 |
| Received | Aug 25, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152401
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.