510(k) K152887 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Crosperio RX PTA Balloon Dilatation Catheter
| Applicant | KANEKA Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Jan 22, 2016 |
| Received | Sep 30, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152887
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.