FDA 510(k), K061851, ZIRKONZAHN ICE

FDA 510(k), K061851, ZIRKONZAHN ICE

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510(K) Number: K061851
Device Name: ZIRKONZAHN ICE
Manufacturer: ZIRKONZAHN GMBH
Device Classification Name: powder, porcelain
Regulation Number: 872.6660
Classification Product Code: EIH
Date Received: 06/30/2006
Decision Date: 09/29/2006
Regulation Medical Specialty: Dental

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