FDA 510(k) Applications Submitted by DIO DEPARTMENT DSI, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K061797 06/26/2006 SM IMPLANT SYSTEMS DIO DEPARTMENT DSI, INC.
K080126 01/17/2008 DIO PROTEM IMPLANT SYSTEM DIO DEPARTMENT DSI, INC.
K080128 01/17/2008 SM-EXTRA WIDE (RBM) IMPLANT SYSTEM DIO DEPARTMENT DSI, INC.
K080129 01/17/2008 SECURE IMPLANT SYSTEM (2.5/3.0MM) DIO DEPARTMENT DSI, INC.
K070568 02/28/2007 DIO PROTEM IMPLANT SYSTEM DIO DEPARTMENT DSI, INC.
K070569 02/28/2007 SM INTERNAL./EXTERNAL IMPLANT SYSTEM DIO DEPARTMENT DSI, INC.
K070570 02/28/2007 DIO IMPLANT SYSTEM DIO DEPARTMENT DSI, INC.
K073070 10/30/2007 DIO BIOTITE-H IMPLANT SYSTEM DIO DEPARTMENT DSI, INC.


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