FDA 510(k) Applications Submitted by ConvaTec, Inc.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K230400 | 02/15/2023 | Cure Catheter Closed System; Cure Dextra Closed System | ConvaTec, Inc. |
| K221593 | 06/02/2022 | Cure Ultra Male, Cure Ultra Female, Cure Ultra Plus | ConvaTec, Inc. |
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