FDA 510(k), K173574, DenSeeMammo
FDA 510(k), K173574, DenSeeMammo
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510(K) Number: K173574
Device Name: DenSeeMammo
Manufacturer: Stephane Ragusa
Device Classification Name: System, Image Processing, Radiological
Regulation Number: LLZ
Classification Product Code: 11/20/2017
Date Received: 06/26/2018
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Radiology
Device Name: DenSeeMammo
Manufacturer: Stephane Ragusa
Device Classification Name: System, Image Processing, Radiological
Regulation Number: LLZ
Classification Product Code: 11/20/2017
Date Received: 06/26/2018
Decision Date: Substantially Equivalent (SESE)
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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