• FDA 510(k) records for MobileRay Pulse SE Digital Imaging System K191503
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FDA 510(k) K130223, RMGI FILL, by Pulpdent Corporation

FDA 510(k) K130223, RMGI FILL, by Pulpdent Corporation

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510(K) Number: K130223
Device Name: RMGI FILL
Manufacturer: Pulpdent Corporation
Device Classification Name: cement, dental
Regulation Number: 872.3275
Classification Product Code: EMA
Date Received: 01/29/2013
Decision Date: 03/29/2013
Regulation Medical Specialty: Dental
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