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
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
- 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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