510(k) K201333 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
SABER .035 PTA Dilatation Catheter
| Applicant | Cordis Corporation, Miami Lakes FL, US |
| Decision | Substantially Equivalent, Sep 11, 2020 |
| Received | May 19, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K201333
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.