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FDA 510(k), K934073, JEDENTAL GLASS IONOMER CEMENT AND LINER
FDA 510(k), K934073, JEDENTAL GLASS IONOMER CEMENT AND LINER
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510(K) Number: K934073
Device Name: JEDENTAL GLASS IONOMER CEMENT AND LINER
Manufacturer: JEDENTAL CO., INC.
Device Classification Name: Cement, Dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 08/20/1993
Decision Date: 01/26/1994
Regulation Medical Specialty: Dental
Device Name: JEDENTAL GLASS IONOMER CEMENT AND LINER
Manufacturer: JEDENTAL CO., INC.
Device Classification Name: Cement, Dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 08/20/1993
Decision Date: 01/26/1994
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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