FDA 510(k) Applications Submitted by AMY E FOWLER

FDA 510(k) Number Submission Date Device Name Applicant
K962065 05/28/1996 3M VITREBOND LIGHT CURE GLASS IONOMER/BASE 3M COMPANY
K963766 09/19/1996 3M PROPLUS SYSTEM 3M COMPANY
K981325 04/13/1998 3M M.G. MATERIAL 3M COMPANY


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