FDA 510(k), K110582, VALO CORDLESS
FDA 510(k), K110582, VALO CORDLESS
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510(K) Number: K110582
Device Name: VALO CORDLESS
Manufacturer:
Device Classification Name: Activator, Ultraviolet, For Polymerization
Regulation Number: 872.6070
Classification Product Code: EBZ
Date Received: 03/01/2011
Decision Date: 04/28/2011
Regulation Medical Specialty: Dental
Device Name: VALO CORDLESS
Manufacturer:
Device Classification Name: Activator, Ultraviolet, For Polymerization
Regulation Number: 872.6070
Classification Product Code: EBZ
Date Received: 03/01/2011
Decision Date: 04/28/2011
Regulation Medical Specialty: Dental