FDA 510(k), K200422, Image Quality Analyzer (IQA)

FDA 510(k), K200422, Image Quality Analyzer (IQA)

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510(K) Number: K200422
Device Name: Image Quality Analyzer (IQA)
Manufacturer: VisionQuest BioMedical, Inc.
Device Classification Name: System, Image Management, Ophthalmic
Regulation Number: 892.2050
Classification Product Code: NFJ
Date Received: 02/20/2020
Decision Date: 12/24/2020
Regulation Medical Specialty: Radiology

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