510(k) K133843 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
SABER PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY DILATATION CATHETER
| Applicant | Cordis Corporation, Fremont CA, US |
| Decision | Substantially Equivalent, Jun 27, 2014 |
| Received | Dec 18, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133843
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jul 19, 2021 | Cordis Corporation Cordis SABER PTA Balloon Dilation Catheter, 4F, REF 48004010X Terminated |
LIT | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.