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FDA 510(k) Applications Submitted by DENPLUS, INC.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K011762
06/07/2001
HI-WAVE; POUR-PLUS
DENPLUS, INC.
K991996
06/14/1999
IMPACT-PLUS, IMPACT-20, DP97, DP97-20, DP-POUR AND DP-REPAIR
DENPLUS, INC.
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