FDA 510(k), K895901, VITA CEREC SET AND VITA CEREC BLOCS
FDA 510(k), K895901, VITA CEREC SET AND VITA CEREC BLOCS
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510(K) Number: K895901
Device Name: VITA CEREC SET AND VITA CEREC BLOCS
Manufacturer: VIDENT
Device Classification Name: material, impression
Regulation Number: 872.3660
Classification Product Code: ELW
Date Received: 10/06/1989
Decision Date: 01/17/1992
Regulation Medical Specialty: Dental
Device Name: VITA CEREC SET AND VITA CEREC BLOCS
Manufacturer: VIDENT
Device Classification Name: material, impression
Regulation Number: 872.3660
Classification Product Code: ELW
Date Received: 10/06/1989
Decision Date: 01/17/1992
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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