510(k) K210626 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
SABER .035 Percutaneous Transluminal Angioplasty (PTA) Dilatation Catheter
| Applicant | Cordis Corporation, Miami Lakes FL, US |
| Decision | Substantially Equivalent, Apr 23, 2021 |
| Received | Mar 2, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K210626
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.