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FDA 510(k), K102341, VIPI BLOCK
FDA 510(k), K102341, VIPI BLOCK
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510(K) Number: K102341
Device Name: VIPI BLOCK
Manufacturer: VIPI INDUSTRIA,COMERCIO,EXPORTACAO E IMPORTACAO DE
Device Classification Name: crown and bridge, temporary, resin
Regulation Number: 872.3770
Classification Product Code: EBG
Date Received: 08/18/2010
Decision Date: 12/16/2010
Regulation Medical Specialty: Dental
Device Name: VIPI BLOCK
Manufacturer: VIPI INDUSTRIA,COMERCIO,EXPORTACAO E IMPORTACAO DE
Device Classification Name: crown and bridge, temporary, resin
Regulation Number: 872.3770
Classification Product Code: EBG
Date Received: 08/18/2010
Decision Date: 12/16/2010
Regulation Medical Specialty: Dental
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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