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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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