FDA 510(k), K083695, TRAXODENT

FDA 510(k), K083695, TRAXODENT

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510(K) Number: K083695
Device Name: TRAXODENT
Manufacturer: PREMIER DENTAL PRODUCTS CO.
Device Classification Name: cord, retraction
Regulation Number:
Classification Product Code: MVL
Date Received: 12/15/2008
Decision Date: 04/28/2009
Regulation Medical Specialty:

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