FDA 510(k) Applications Submitted by UroCure LLC
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K222468 | 08/16/2022 | ArcTO Transobturator Sling System | UroCure LLC |
| K183134 | 11/13/2018 | ArcTV Transvaginal Sling System | UroCure LLC |
| K222293 | 08/01/2022 | ArcSP Suprapubic Sling System | UroCure LLC |
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