FDA 510(k), K060149, SUNIPAN IMAGING SYSTEM & ACCESSORIES

FDA 510(k), K060149, SUNIPAN IMAGING SYSTEM & ACCESSORIES

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510(K) Number: K060149
Device Name: SUNIPAN IMAGING SYSTEM & ACCESSORIES
Manufacturer:
Device Classification Name: System, X-Ray, Extraoral Source, Digital
Regulation Number: 872.1800
Classification Product Code: MUH
Date Received: 01/20/2006
Decision Date: 02/03/2006
Regulation Medical Specialty: Dental
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