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FDA 510(k), K140132, BIODENTINE
FDA 510(k), K140132, BIODENTINE
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510(K) Number: K140132
Device Name: BIODENTINE
Manufacturer: SEPTODONT
Device Classification Name: resin, root canal filling
Regulation Number: 872.3820
Classification Product Code: KIF
Date Received: 01/17/2014
Decision Date: 06/27/2014
Regulation Medical Specialty: Dental
Device Name: BIODENTINE
Manufacturer: SEPTODONT
Device Classification Name: resin, root canal filling
Regulation Number: 872.3820
Classification Product Code: KIF
Date Received: 01/17/2014
Decision Date: 06/27/2014
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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