FDA 510(k) Applications Submitted by PAUL W EVANS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K002901	09/18/2000	KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER	THE KENDALL COMPANY
K990500	02/17/1999	KENDALL ULTRAMER COUDE FOLEY CATHETER, MODEL 1416C, KENDALL CURITY COUDE FOLEY CATHETER TRAY, MODEL 6946C	THE KENDAL CO.
K070653	03/09/2007	KENDALL KERLIX ANTIMICROBIAL SUPER SPONGE DRESSING FOR OTC USE, MODEL 6662	TYCO HEALTHCARE
K070685	03/12/2007	KENDALL ANTIMICROBIAL DRAIN DRESSING FOR OTC USE, MODEL 6662	TYCO HEALTHCARE
K992079	06/21/1999	KENDALL MODEL 7325 SCD RESPONSE COMPRESSION SYSTEM, MODEL 7325	THE KENDALL COMPANY, L.P.
K061936	07/10/2006	KENDALL ARGYLE NEONATAL/PEDIATRIC PICC, MODEL 43311	THE KENDALL COMPANY
K042461	09/10/2004	KENDALL ARGYLE 2 FR DOUBLE LUMEN NEONATAL/PEDIATRIC PICC, MODEL 43304	KENDALL
K973546	09/18/1997	KENDALL FAST-CATH PRE LUBRICATED URETHRAL CATHETER	KENDALL HEALTHCARE PRODUCTS CO. DIV.OF TYCO HEALTH