FDA 510(k) Applications Submitted by LOUISVILLE LABORATORIES, INC.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K960882	02/20/1996	CONTROL SYRINGE	LOUISVILLE LABORATORIES, INC.
K963076	08/07/1996	LAPAROSCOPIC BONE ANCHORED URETHROPEXY INSTRUMENT TRAY	LOUISVILLE LABORATORIES, INC.
K955535	12/05/1995	LOUISVILLE LABS OXYGEN HEAD TENT	LOUISVILLE LABORATORIES, INC.
K980123	01/14/1998	CARTER-THOMASON NEEDLE-POINT SUTURE PASSER INSTRUMENT SET	LOUISVILLE LABORATORIES, INC.
K971791	05/15/1997	VAGINAL SUTURING KIT FOR LAPAROTOMY BLADDER NECK SUSPENSION	LOUISVILLE LABORATORIES, INC.
K971796	05/15/1997	LAPAROTOMY BLADDER NECK SUSPENSION KIT WITH BONE ANCHORS	LOUISVILLE LABORATORIES, INC.
K971797	05/15/1997	LAPAROSCOPIC BLADDER NECK SUSPENSION KIT	LOUISVILLE LABORATORIES, INC.
K971801	05/15/1997	LAPAROTOMY BLADDER NECK SUSPENSION KIT	LOUISVILLE LABORATORIES, INC.
K971802	05/15/1997	VAGINAL SUTURING KIT FOR BLADDER NECK SUSPENSION	LOUISVILLE LABORATORIES, INC.