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
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
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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