510(k) K171612 ยท DQY Catheter, Percutaneous
ACUITY Pro Lead Delivery System
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Jun 30, 2017 |
| Received | Jun 1, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K171612
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.