FDA 510(k) Applications Submitted by JULIE A BEAUMONT

FDA 510(k) Number	Submission Date	Device Name	Applicant
K990547	02/22/1999	PILLING WECK SURGICAL Y STENT FORCEPS	PILLING WECK, INC.
K010797	03/16/2001	RUSCH MILLER-ABBOTT TUBE	RUSCH INTL.
K010798	03/16/2001	RUSCH CANTOR TUBE	RUSCH INTL.
K011121	04/12/2001	RUSCH PERCUTANEOUS NEPHROSTOMY CATHETER SETS	RUSCH INTL.
K011122	04/12/2001	BALLPEN SPINAL NEEDLE W/WO INTRODUCER	RUSCH INTL.
K011210	04/19/2001	THE PERCUQUICK SET FOR PERCUTANEOUS DILATION TRACHEOSTOMY	RUSCH INTL.
K991647	05/13/1999	TFX MEDICAL INTRODUCER KIT	TFX MEDICAL GROUP
K992664	08/09/1999	TFX MEDICAL STYLET CATHETER	TFX MEDICAL GROUP
K993063	09/13/1999	RUSCH BRILLANT SILICONE FOLEY	RUSCH INTL.