FDA 510(k) Applications Submitted by Mark Nelson

FDA 510(k) Number	Submission Date	Device Name	Applicant
K050023	01/05/2005	SECURELOC; ADVANCINTRODUCER	SPECIALIZED HEALTH PRODUCTS, INC.
K070449	02/15/2007	LUMILOC (TM) SAFETY INTRODUCER NEEDLE	SPECIALIZED HEALTH PRODUCTS INTERNATIONAL, INC.
K050600	03/09/2005	MINILOC SAFETY INFUSION SET	SPECIALIZED HEALTH PRODUCTS, INTL.
K101261	05/05/2010	CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000	C.R. BARD, INC.
K042234	08/18/2004	MODIFICATION TO: LIFTLOC SAFTEY INFUSION SET	SPECIALTY HEALTH PRODUCTS, INC.
K013394	10/15/2001	LIFTLOC SAFETY INFUSION SET	SPECIALIZED HEALTH PRODUCTS, INC.
K073050	10/29/2007	SAFESTEP MAX POWER-INJECTABLE INFUSION SET	SPECIALIZED HEALTH PRODUCTS INTERNATIONAL, INC.