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FDA 510(k) Applications Submitted by LINDA RUEDY
FDA 510(k) Number
Submission Date
Device Name
Applicant
K060248
01/31/2006
ULTRATINE TRANSBLEPH
COAPT SYSTEMS, INC.
K060249
01/31/2006
ULTRATINE FOREHEAD
COAPT SYSTEMS, INC.
K050611
03/09/2005
ENDOTINE RIBBON
COAPT SYSTEMS, INC.
K060828
03/27/2006
MODIFICATION TO ENDOTINE RIBBON
COAPT SYSTEMS, INC.
K080956
04/03/2008
MODIFICATION TO VF GEL PLUS
COAPT SYSTEMS, INC.
K051415
06/01/2005
ENDOTINE RIBBON
COAPT SYSTEMS, INC.
K071663
06/18/2007
VF GEL PLUS
COAPT SYSTEMS, INC.
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