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FDA 510(k), K173274, Ceevra Reveal 2.0
FDA 510(k), K173274, Ceevra Reveal 2.0
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510(K) Number: K173274
Device Name: Ceevra Reveal 2.0
Manufacturer: Ceevra, Inc.
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 10/12/2017
Decision Date: 07/10/2018
Regulation Medical Specialty: Radiology
Device Name: Ceevra Reveal 2.0
Manufacturer: Ceevra, Inc.
Device Classification Name: System, Image Processing, Radiological
Regulation Number: 892.2050
Classification Product Code: LLZ
Date Received: 10/12/2017
Decision Date: 07/10/2018
Regulation Medical Specialty: Radiology
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- 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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