510(k) K160004 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
Crosstella OTW
| Applicant | KANEKA Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Apr 29, 2016 |
| Received | Jan 4, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K160004
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.