Convatec, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest Approval2023-11-08
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K230400 | Cure Catheter Closed System; Cure Dextra Closed System | EZD | 2023-11-08 | View |
| 510(k) | K221593 | Cure Ultra Male, Cure Ultra Female, Cure Ultra Plus | EZD | 2022-11-17 | View |
No matching devices.