510(k) K071042 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
POLARCATH PERIPHERAL DILATATION SYSTEM
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Jun 13, 2007 |
| Received | Apr 12, 2007 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K071042
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.