FDA 510(k), K123402, DIAGNOCAM

FDA 510(k), K123402, DIAGNOCAM

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510(K) Number: K123402
Device Name: DIAGNOCAM
Manufacturer: KALTENBACH & VOIGT GMBH
Device Classification Name: Caries Detector, Laser Light, Transmission
Regulation Number: 872.1745
Classification Product Code: NTK
Date Received: 11/05/2012
Decision Date: 09/24/2013
Regulation Medical Specialty: Dental

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