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Centervue S.P.A.

FDA 510(k) & PMA Approved Devices — 10 products

Total Devices10
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K243504 MAIA (AHMACME001)MYC2025-03-17 View
510(k) K234076 iCare ALTIUS CWNFJ2024-08-22 View
510(k) K213705 DRSplusMYC2021-12-21 View
510(k) K211328 EIDON FA, EIDON, EIDON AF, EIDON UWFLMYC2021-08-19 View
510(k) K192113 DRSplusMYC2019-11-15 View
510(k) K180526 EIDON FAMYC2018-07-16 View
510(k) K180293 Retia 2MYC2018-05-30 View
510(k) K153181 MAIAMYC2016-06-08 View
510(k) K101935 CENTERVUE DIGITAL RETINOGRAPHY SYSTEMHKI2010-10-27 View
510(k) K092187 MAIA, MODEL 1HPT2010-05-27 View
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