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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