FDA 510(k) Applications Submitted by THE KENDALL COMPANY

FDA 510(k) Number	Submission Date	Device Name	Applicant
K011283	04/27/2001	MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE	THE KENDALL COMPANY
K002902	09/18/2000	TANDEM-CATH 10 FR. CATHETER SYSTEM, MODEL MULTIPLE CODE NUMBERS	THE KENDALL COMPANY
K003313	10/23/2000	FILAC FAS TEMP ELECTRONIC THERMOMETER	THE KENDALL COMPANY
K011941	06/21/2001	EXCILON AMD ANTIMICROBIAL SPONGE MODEL #7088	THE KENDALL COMPANY
K002901	09/18/2000	KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER	THE KENDALL COMPANY
K061936	07/10/2006	KENDALL ARGYLE NEONATAL/PEDIATRIC PICC, MODEL 43311	THE KENDALL COMPANY
K020089	01/10/2002	MAHURKAR TRIPLE LUMEN CATHETER, 12 FR	THE KENDALL COMPANY
K030209	01/21/2003	MAHURKAR OPLUS CATHETER, MODEL 13.5 FR	THE KENDALL COMPANY