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FDA 510(k), K051866, PREMIER TEMPORARY CEMENT
FDA 510(k), K051866, PREMIER TEMPORARY CEMENT
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510(K) Number: K051866
Device Name: PREMIER TEMPORARY CEMENT
Manufacturer: PREMIER DENTAL PRODUCTS CO.
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 07/11/2005
Decision Date: 09/06/2005
Regulation Medical Specialty: Dental
Device Name: PREMIER TEMPORARY CEMENT
Manufacturer: PREMIER DENTAL PRODUCTS CO.
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 07/11/2005
Decision Date: 09/06/2005
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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