FDA 510(k) Applications Submitted by DAN CLARK

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020333	01/31/2002	ATRION MEDICAL QL FLUID DISPENSING SYRINGE	ATRION MEDICAL PRODUCTS, INC.
K060643	03/10/2006	QL LOCKING SYRINGE	ATRION MEDICAL PRODUCTS, INC.
K041158	05/03/2004	ATRION EPIDURAL ANESTHESIA KIT WITH ATRION NEEDLEVISE SHARPS SECURING SYSTEM	ATRION MEDICAL PRODUCTS, INC.
K962151	06/04/1996	RYDER LACRIMAL INTUBATIONSET	RYDER INTL. CORP.
K962611	07/03/1996	BARD EAGLE INFLATION DEVICE	RYDER INTL. CORP.
K973633	07/17/1997	ATRION MEDICAL PRODUCTS LACRIMAL INTUBATION SET	ATRION MEDICAL PRODUCTS, INC.
K122190	07/24/2012	PRELUDE 7F SHORT SHEATH INTRODUCER	MERIT MEDICAL SYSTEMS, INC.
K972964	08/11/1997	ATRION MEDICAL BALLOON CATHETER INFLATION DEVICE	ATRION MEDICAL PRODUCTS, INC.
K032840	09/11/2003	ATRION MEDICAL QL INFLATION DEVICE	ATRION MEDICAL PRODUCTS, INC.
K973872	10/10/1997	ATRION MEDICAL COATED LACRIMAL INTUBATION SET	ATRION MEDICAL PRODUCTS, INC.
K043249	11/23/2004	ATRION NEEDLEVISE LARGE-BORE SHARPS SECURING DEVICE	ATRION MEDICAL PRODUCTS, INC.
K971100	03/26/1997	ATRION MEDICAL AUTOGENOUS TISSUE COLLECTOR	ATRION MEDICAL PRODUCTS, INC.
K230266	01/31/2023	Orchid Safety Release Valve	Linear Health Sciences, LLC
K212064	07/02/2021	Orchid Safety Release Valve(TM)	Linear Health Sciences, LLC
K232094	07/13/2023	Orchid Safety Release ValveTM	Linear Health Sciences LLC