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FDA 510(k), K042200, MI PASTE
FDA 510(k), K042200, MI PASTE
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$149.00 USD
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510(K) Number: K042200
Device Name: MI PASTE
Manufacturer: GC AMERICA, INC.
Device Classification Name: agent, polishing, abrasive, oral cavity
Regulation Number: 872.6030
Classification Product Code: EJR
Date Received: 08/13/2004
Decision Date: 10/20/2004
Regulation Medical Specialty: Dental
Device Name: MI PASTE
Manufacturer: GC AMERICA, INC.
Device Classification Name: agent, polishing, abrasive, oral cavity
Regulation Number: 872.6030
Classification Product Code: EJR
Date Received: 08/13/2004
Decision Date: 10/20/2004
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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