FDA 510(k) Applications for Medical Device Product Code "EZC"
(Catheter, Coude)

FDA 510(k) Number Applicant Device Name Decision Date
K173596 Teleflex Medical Rusch Intermittent Urethral Catheters 01/29/2018
K222279 Teleflex Medical Rusch Intermittent Urethral Catheters 08/29/2022


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