FDA 510(k) Applications Submitted by UroGen Pharma Ltd.

FDA 510(k) Number Submission Date Device Name Applicant
K180354 02/08/2018 UroGen Ureteral Catheter UroGen Pharma Ltd.
K180345 02/08/2018 Uroject12 Syringe Lever UroGen Pharma Ltd.
K190987 04/15/2019 Uroject12 Syringe Lever UroGen Pharma Ltd.


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