FDA 510(k) Applications Submitted by Liz Schindel
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180345 | 02/08/2018 | Uroject12 Syringe Lever | UroGen Pharma Ltd. |
| K190987 | 04/15/2019 | Uroject12 Syringe Lever | UroGen Pharma Ltd. |
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