FDA 510(k) Applications Submitted by MC3 Incorporated

FDA 510(k) Number Submission Date Device Name Applicant
K180151 01/19/2018 MC3 Jugular Dual Lumen Catheter MC3 Incorporated
K191935 07/19/2019 Nautilus Smart ECMO Module MC3 Incorporated
K182914 10/18/2018 MC3 Vascular Access Kit 21030 MC3 Incorporated
K171610 06/01/2017 MC3 QuickFlow Dual Lumen Catheter MC3 Incorporated


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact