FDA 510(k), K150432, IDODENTINE DISC, IDODENTINE BLOCK
FDA 510(k), K150432, IDODENTINE DISC, IDODENTINE BLOCK
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510(K) Number: K150432
Device Name: IDODENTINE DISC, IDODENTINE BLOCK
Manufacturer: UNION DENTAL S.A.
Device Classification Name: crown and bridge, temporary, resin
Regulation Number: 872.3770
Classification Product Code: EBG
Date Received: 02/19/2015
Decision Date: 08/14/2015
Regulation Medical Specialty: Dental
Device Name: IDODENTINE DISC, IDODENTINE BLOCK
Manufacturer: UNION DENTAL S.A.
Device Classification Name: crown and bridge, temporary, resin
Regulation Number: 872.3770
Classification Product Code: EBG
Date Received: 02/19/2015
Decision Date: 08/14/2015
Regulation Medical Specialty: Dental
- 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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