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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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