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FDA 510(k), K103556, IPS E.MAX CAD CRYSTALL / CONNECT AND IPS E.MAX CAD CRYSTAL / ADD-ON CONNECT (FOR CAD-ON TECHNIQUE)
FDA 510(k), K103556, IPS E.MAX CAD CRYSTALL / CONNECT AND IPS E.MAX CAD CRYSTAL / ADD-ON CONNECT (FOR CAD-ON TECHNIQUE)
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510(K) Number: K103556
Device Name: IPS E.MAX CAD CRYSTALL / CONNECT AND IPS E.MAX CAD CRYSTAL / ADD-ON CONNECT (FOR CAD-ON TECHNIQUE)
Manufacturer: IVOCLAR VIVADENT, INC.
Device Classification Name: powder, porcelain
Regulation Number: 872.6660
Classification Product Code: EIH
Date Received: 12/02/2010
Decision Date: 04/13/2011
Regulation Medical Specialty: Dental
Device Name: IPS E.MAX CAD CRYSTALL / CONNECT AND IPS E.MAX CAD CRYSTAL / ADD-ON CONNECT (FOR CAD-ON TECHNIQUE)
Manufacturer: IVOCLAR VIVADENT, INC.
Device Classification Name: powder, porcelain
Regulation Number: 872.6660
Classification Product Code: EIH
Date Received: 12/02/2010
Decision Date: 04/13/2011
Regulation Medical Specialty: Dental
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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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