510(k) K201377 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
SABERX RADIANZ Percutaneous Transluminal Angioplasty Dilatation Catheter
| Applicant | Cordis Corporation, Miami Lakes FL, US |
| Decision | Substantially Equivalent, Oct 9, 2020 |
| Received | May 26, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201377
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.