FDA 510(k), K143499, eCligner

FDA 510(k), K143499, eCligner

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510(K) Number: K143499
Device Name: eCligner
Manufacturer: Tae Weon Kim
Device Classification Name: Aligner, Sequential
Regulation Number: NXC
Classification Product Code: 12/10/2014
Date Received: 10/09/2015
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Dental
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