Company ยท US
Cagent Vascular, LLC
FDA 510(k) clearances and medical device recalls filed under this name, 2017 to 2022. Name variants (Inc, Corp, punctuation) are merged.
5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
| Code | Device | Records |
|---|---|---|
| PNO | Catheter, Percutaneous, Cutting/Scoring | 5 |
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| May 4, 2022 | K220704 | Serranator PTA Serration Balloon Catheter Cagent Vascular, LLC | PNO |
| Dec 15, 2021 | K213728 | Serranator PTA Serration Balloon Catheter Cagent Vascular, LLC | PNO |
| Dec 22, 2020 | K203437 | Serranator PTA Serration Balloon Catheter Cagent Vascular, LLC | PNO |
| Apr 15, 2020 | K193181 | Serranator PTA Serration Balloon Catheter Cagent Vascular, LLC | PNO |
| Feb 13, 2017 | K163380 | Serranator Alto PTA Serration Balloon Catheter Cagent Vascular, LLC | PNO |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||