FDA 510(k) Applications for Medical Device Product Code "EZC"
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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 |