510(k) K060959 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
SYMMETRY BALLOON DILATATION CATHETER
| Applicant | Boston Scientific Corporation, Maple Grove MN, US |
| Decision | Substantially Equivalent, Apr 12, 2006 |
| Received | Apr 7, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060959
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.