FDA 510(k) Applications Submitted by ALAN P SCHWARTZ

FDA 510(k) Number	Submission Date	Device Name	Applicant
K091364	05/08/2009	DICOMPACS, MODEL 5.2, DICOMPACS DX-R, MODEL 1.4	OEHM UND REHBEIN GMBH
K073249	11/19/2007	SOLARIS NT1 AND NT1A HANDHELD PULSE OXIMETERS WITH SENSOR ACCESSORIES	SOLARIS MEDICAL TECHNOLOGY, INC.
K011860	06/14/2001	KEYST0NE MEDICAL PICC CATHETER	KEYSTONE MEDICAL
K001958	06/27/2000	KEYSTONE MEDICAL SCHON XL SOFT-LINE DOUBLE LUMENT CATHETER. KEYSTONE MEDICAL 12 F DUO-FLOW AND 14F DUO-FLOW 400 XL CATH	KEYSTONE MEDICAL
K042213	08/16/2004	PRE-POWDERED NON-STERILE VINYL EXAMINATION GLOVES	SHANDONG PERFECT PLASTIC CO., LTD.
K042214	08/16/2004	POWDER-FREE NON-STERILE VINYL EXAMINATION GLOVES	SHANDONG PERFECT PLASTIC CO., LTD.
K072859	10/05/2007	ATRAMAT PGLA90 POLY(GLYCOLIDE-CO-L-LACTIDE) SURGICAL SUTURES	INTERNACIONAL FARMACEUTICA, S.A. DE C.V.