Convatec, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 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 |
| 510(k) | K123481 | AQUACEL AG FOAM HYDROFIBER FOAM DRESSING WITH SILVER, ADHESIVE AND NON ADHESIVE | FRO | 2013-06-06 | View |
| 510(k) | K121275 | AQUACEL AG EXTRA HYDROFIBER DRESSING WITH SILVER AND STRENGTHENING FIBER | FRO | 2012-07-25 | View |
| 510(k) | K112342 | FLEXI-SEAL SIGNAL FECAL MANAGEMENT SYSTEM | KNT | 2012-04-26 | View |
| 510(k) | K111365 | VITALA CONTINENCE CONTROL DEVICE | EZQ | 2011-08-19 | View |
| 510(k) | K102536 | VITALA CONTINENCE CONTROL DEVICE | EZQ | 2010-12-01 | View |
No matching devices.
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