510(k) K141150 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
PTA BALLOON DILATATION CATHETER
| Applicant | Boston Scientific Corp, Maple Grove MN, US |
| Decision | Substantially Equivalent, Sep 25, 2014 |
| Received | May 5, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141150
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.