510(k) K163479 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
R2P Metacross RX
| Applicant | KANEKA Corporation, Tokyo, JP |
| Decision | Substantially Equivalent, Jan 11, 2017 |
| Received | Dec 12, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K163479
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.