FDA 510(k) Applications Submitted by CENTERVUE SPA

FDA 510(k) Number Submission Date Device Name Applicant
K092187 07/21/2009 MAIA, MODEL 1 CENTERVUE SPA
K211328 05/03/2021 EIDON FA, EIDON, EIDON AF, EIDON UWFL CenterVue SpA
K213705 11/24/2021 DRSplus CenterVue SpA
K180293 02/01/2018 Retia 2 CenterVue SpA
K150320 02/09/2015 COMPASS CENTERVUE SPA
K180526 02/27/2018 EIDON FA CenterVue SpA
K192113 08/05/2019 DRSplus CenterVue SpA
K153181 11/03/2015 MAIA CENTERVUE SPA
K101935 07/12/2010 CENTERVUE DIGITAL RETINOGRAPHY SYSTEM CENTERVUE SPA
K142047 07/28/2014 EIDON CENTERVUE SPA
K133758 12/11/2013 CENTERVUE MACULAR INTEGRITY ASSESSMENT CENTERVUE SPA


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