FDA 510(k), K080749, RADIANCE

FDA 510(k), K080749, RADIANCE

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510(K) Number: K080749
Device Name: RADIANCE
Manufacturer: AMERICAN ORTHODONTICS
Device Classification Name: bracket, ceramic, orthodontic
Regulation Number: 872.5470
Classification Product Code: NJM
Date Received: 03/17/2008
Decision Date: 08/04/2008
Regulation Medical Specialty: Dental
  • Status: Pending Fast-Track Request
  • Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity

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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