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Optos Plc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories2
Latest FDA decision2024-05-09
TypeNumberDevice NameCodeDateActions
510(k) K233602 P200TE (A10700)OBO2024-05-09 View
510(k) K231673 P200TE (A10700)OBO2023-08-18 View
510(k) K190732 P200TxEOBO2019-07-31 View
510(k) K173707 P200TEOBO2018-02-28 View
510(k) K162039 OptosAdvance 4.0 SoftwareNFJ2017-02-08 View

Related Clinical Trials

NCT05844852P200TE US Reference Database StudyCOMPLETEDNCT06269666P200TxE Diseased Eye Image CollectionCOMPLETEDNCT05961332COmparison of Clarus and Optos Ultrawide Field Imaging Systems for Geographic AtrophyCOMPLETEDNCT06380075COmparison of Clarus and Optos Ultrawide Field Imaging Systems for Inherited Retinal DiseaseRECRUITINGNCT07568704Image Evaluation of Intalight Dream OCTA Scans With Optos FA & ICGA ImagesRECRUITINGNCT07747662Adaptive Optics Scanning Light Ophthalmoscopy (AOSLO) and Microperimetry (MP) Sub-studyENROLLING_BY_INVITATION
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