510(k) K143193 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Symmetry and Symmetry Stiff Shaft Balloon Dilatation Catheters
| Applicant | Boston Scientific, Maple Grove MN, US |
| Decision | Substantially Equivalent, Jul 24, 2015 |
| Received | Nov 6, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143193
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.