FDA 510(k), K051664, SCAN300FP / RETROPAN (VDC)
FDA 510(k), K051664, SCAN300FP / RETROPAN (VDC)
Device Name: SCAN300FP / RETROPAN (VDC)
Manufacturer:
Device Classification Name: System, X-Ray, Extraoral Source, Digital
Regulation Number: 872.1800
Classification Product Code: MUH
Date Received: 06/22/2005
Decision Date: 07/20/2005
Regulation Medical Specialty: Dental
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