FDA 510(k), K123265, RMGI LOW VISCOSITY

FDA 510(k), K123265, RMGI LOW VISCOSITY

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510(K) Number: K123265
Device Name: RMGI LOW VISCOSITY
Manufacturer: PULPDENT CORPORATION
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 10/19/2012
Decision Date: 12/07/2012
Regulation Medical Specialty: Dental
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