510(k) K150303 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
XXL Vascular Balloon Dilatation Catheter
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Jun 15, 2015 |
| Received | Feb 6, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150303
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.