FDA 510(k) Applications Submitted by BRUCE R LESTER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K050343	02/11/2005	REPROCESSED HARMONIC SCALPELS	STERILMED, INC.
K041127	04/30/2004	MODIFICATION TO: REPROCESSED OXIMAX PULSE OXIMETER SENSORS	STERILMED, INC.
K042648	09/28/2004	REPROCESSED COLD BIOPSY FORCEPS	STERILMED, INC.
K043453	12/15/2004	STERILEMED REPROCESSED IVUS IMAGING CATHETER	STERILMED, INC.
K050136	01/21/2005	REPROCESSED HOT BIOPSY FORCEPS	STERILMED, INC.
K051220	05/12/2005	REPROCESSED DEFLECTABLE ELECTROPHYSIOLOGY DIAGNOSTIC CATHETERS	STERILMED, INC.
K053188	11/15/2005	REPROCESSED BALOON INFLATION DEVICE	STERILMED, INC.
K043513	12/20/2004	STERILMED REPROCESSED DEFLECTABLE ELECTROPHYSIOLOGY DIAGNOSTIC CATHETER	STERILMED, INC.
K043592	12/29/2004	REPROCESSED ENDOSCOPIC TROCAR	STERILMED, INC.