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FDA 510(k), K994435, OPC 3G ALL-CERAMIC SYSTEM, CORE AND OVERLAY PORCELAINS
FDA 510(k), K994435, OPC 3G ALL-CERAMIC SYSTEM, CORE AND OVERLAY PORCELAINS
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510(K) Number: K994435
Device Name: OPC 3G ALL-CERAMIC SYSTEM, CORE AND OVERLAY PORCELAINS
Manufacturer: JENERIC/PENTRON, INC.
Device Classification Name: powder, porcelain
Regulation Number: 872.6660
Classification Product Code: EIH
Date Received: 12/30/1999
Decision Date: 02/10/2000
Regulation Medical Specialty: Dental
Device Name: OPC 3G ALL-CERAMIC SYSTEM, CORE AND OVERLAY PORCELAINS
Manufacturer: JENERIC/PENTRON, INC.
Device Classification Name: powder, porcelain
Regulation Number: 872.6660
Classification Product Code: EIH
Date Received: 12/30/1999
Decision Date: 02/10/2000
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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