FDA 510(k) Applications Submitted by James G. Ottinger
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K180354 | 02/08/2018 | UroGen Ureteral Catheter | UroGen Pharma Ltd. |
| K203321 | 11/12/2020 | Cystoject Syringe Lever | UroGen Pharma Ltd |
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