510(k) K132430 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
STERLING OVER-THE-WIRE (OTW) PTA BALLOON DILATATION CATHETER
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Oct 17, 2013 |
| Received | Aug 5, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132430
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.