510(k) K143652 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Vector PTA Balloon Dilatation Catheter
| Applicant | Vector Corporation, LLC, New York NY, US |
| Decision | Substantially Equivalent, Feb 26, 2015 |
| Received | Dec 23, 2014 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K143652
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.