FDA 510(k) Applications Submitted by MARY L ARMSTRONG

FDA 510(k) Number	Submission Date	Device Name	Applicant
K100193	01/22/2010	OTOMAG BONE CONDUCTION HEARING SYSTEM	SOPHONO, INC
K960974	03/11/1996	COBE CENTURY PERFUSION PUMP	COBE CARDIOVASCULAR, INC.
K971669	05/06/1997	COBE HVR 4000 FILTERED AND NONFILTERED HARDSHELL VENOUS RESERVOIR	COBE CARDIOVASCULAR, INC.
K962689	07/11/1996	COBE BRAT 2 AUTOLOGOUS BLOOD SALVAGE SYSTEM WITH MODIFIED PLASMA RECOVERY PROGRAM (PRP)	COBE CARDIOVASCULAR, INC.
K963518	09/03/1996	COBE OPTIMA XP HOLLOW FIBER MEMBRANE OXYGENATOR	COBE CARDIOVASCULAR, INC.
K964043	10/09/1996	COBE OPTIMA AND COBE CML DUO MEMBRANE OXYGENATORS	COBE CARDIOVASCULAR, INC.
K103714	12/21/2010	ENCORE ACCLAIM STERILE POWDER-FREE LATEX SURGICAL GLOVES, TESTED FOR USE WITH CHEMOTHERA	ANSELL HEALTHCARE PRODUCTS, LLC