510(k) K221832 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
SABER .014 PTA Dilatation Catheter; SABERX .014 PTA Dilatation Catheter
| Applicant | Cordis US Corp, Miami Lakes FL, US |
| Decision | Substantially Equivalent, Aug 22, 2022 |
| Received | Jun 23, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K221832
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.