FDA 510(k), K190948, Magic Clear Aligners

FDA 510(k), K190948, Magic Clear Aligners

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510(K) Number: K190948
Device Name: Magic Clear Aligners
Manufacturer: Voodoo Manufacturing, Inc.
Device Classification Name: aligner, sequential
Regulation Number: 872.5470
Classification Product Code: NXC
Date Received: 04/11/2019
Decision Date: 05/09/2019
Regulation Medical Specialty: Dental

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