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FDA 510(k), K101787, DUOLINK II
FDA 510(k), K101787, DUOLINK II
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510(K) Number: K101787
Device Name: DUOLINK II
Manufacturer: BISCO, INC.
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 06/25/2010
Decision Date: 10/08/2010
Regulation Medical Specialty: Dental
Device Name: DUOLINK II
Manufacturer: BISCO, INC.
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 06/25/2010
Decision Date: 10/08/2010
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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