FDA 510(k) Applications Submitted by Jennifer Tvrdik
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K242173 | 07/24/2024 | Retrace Ureteral Access Sheath (ASXL10, ASXL12, ACXL10, ACXL12, AXXL10, AXXL12, ALXL10, ALXL12) | Coloplast Corp. |
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