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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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