Cerenovus, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
Total Devices9
Categories3
Latest Approval2025-08-22
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K251828 | CEREGLIDE 71 Catheter System; Cerenovus Aspiration Tubing Set | NRY | 2025-08-22 | View |
| 510(k) | K241244 | CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter | QJP | 2024-10-16 | View |
| 510(k) | K241221 | CEREGLIDE 42 Intermediate Catheter; CEREGLIDE 57 Intermediate Catheter; Cerenovus Aspiration Tubing Set | NRY | 2024-10-16 | View |
| 510(k) | K233982 | CEREGLIDE 92 Catheter System | QJP | 2024-05-09 | View |
| 510(k) | K233988 | Cerenovus Large Bore Catheter; Cerenovus Aspiration Tubing Set | NRY | 2024-01-17 | View |
| 510(k) | K230726 | CEREGLIDE 92 Intermediate Catheter | QJP | 2023-11-29 | View |
| 510(k) | K221930 | CEREGLIDE 71 Intermediate Catheter | QJP | 2023-03-09 | View |
| 510(k) | K221934 | CEREGLIDE 71 Intermediate Catheter; Cerenovus Aspiration Tubing Set | NRY | 2023-03-09 | View |
| PMA | P990040 | tissue adhesive for use in embolization of brain arteriovenous malformations | KGG | 2016-12-14 | View |
No matching devices.