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FDA 510(k), K070854, GC MI PASTE PLUS
FDA 510(k), K070854, GC MI PASTE PLUS
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510(K) Number: K070854
Device Name: GC MI PASTE PLUS
Manufacturer: GC AMERICA, INC.
Device Classification Name: agent, polishing, abrasive, oral cavity
Regulation Number: 872.6030
Classification Product Code: EJR
Date Received: 03/28/2007
Decision Date: 04/12/2007
Regulation Medical Specialty: Dental
Device Name: GC MI PASTE PLUS
Manufacturer: GC AMERICA, INC.
Device Classification Name: agent, polishing, abrasive, oral cavity
Regulation Number: 872.6030
Classification Product Code: EJR
Date Received: 03/28/2007
Decision Date: 04/12/2007
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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