510(k) K171452 ยท DQY Catheter, Percutaneous
MAMBA and MAMBA FLEX Microcatheters
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Aug 21, 2017 |
| Received | May 17, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171452
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.