FDA 510(k) Applications Submitted by JOHN CADWELL JR.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K133355	10/31/2013	CADWELL FLEX EEG/PSG	CADWELL INDUSTRIES, INC.
K091022	04/09/2009	MODIFICATION TO RESERT XL HLD HIGH LEVEL DISINFECTANT	STERIS Corporation
K990188	01/20/1999	INTUITIVE SURGICAL STEREO VIEW ENDOSCOPIC SYSTEM, MODEL SVS-1	INTUITIVE SURGICAL, INC.
K080420	02/15/2008	RESERT XL HLD HIGH LEVEL DISINFECTANT	STERIS Corporation
K090371	02/13/2009	VIS-U-ALL LOW TEMPERATURE TYVEK STERILIZATION POUCH FOR V-PRO 1 STERILIZATION SYSTEM	STERIS Corporation
K083643	12/09/2008	VERIFY 275F GRAVITY INDICATORS	STERIS Corporation
K083665	12/10/2008	VERIFY SCBI 275F 3-10	STERIS Corporation