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FDA 510(k), K001730, GC FUJICEM
FDA 510(k), K001730, GC FUJICEM
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510(K) Number: K001730
Device Name: GC FUJICEM
Manufacturer: GC AMERICA, INC.
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 06/07/2000
Decision Date: 07/17/2000
Regulation Medical Specialty: Dental
Device Name: GC FUJICEM
Manufacturer: GC AMERICA, INC.
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 06/07/2000
Decision Date: 07/17/2000
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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