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Denplus, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K011762 HI-WAVE; POUR-PLUSEBI2001-08-23 View
510(k) K991996 IMPACT-PLUS, IMPACT-20, DP97, DP97-20, DP-POUR AND DP-REPAIREBI1999-09-08 View
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