FDA 510(k) Applications Submitted by PAUL DIAS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K970056	01/07/1997	SOLOS, CIDEO CAMERA REPLACEMENT CABLE, 800/900 SERIES	WOODBINE OPTICAL CORP.
K010257	01/29/2001	ZOLL M SERIES	ZOLL MEDICAL CORP.
K990762	03/08/1999	ZOLL M SERIES WITH RECTILINEAR BI-PHASIC OPTION (M SERIES BI-PHASIC)	ZOLL MEDICAL CORP.
K100654	03/08/2010	ZOLL PROPAQ MD	ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS
K991556	05/04/1999	ZOLL M SERIES 12SL ANALYSIS OPTION	ZOLL MEDICAL CORP.
K011388	05/07/2001	ZOLL PAD	ZOLL MEDICAL CORP.
K011541	05/18/2001	ZOLL PAD WITH CPR AID	ZOLL MEDICAL CORP.
K011865	06/14/2001	ZOLL M SERIES IBP OPERATION; ZOLL M SERIES TEMPERATURE OPTION	ZOLL MEDICAL CORP.
K002029	07/03/2000	ZOLL M SERIES NIBP OPTION, MODEL MSERIES NIBP OPTION	ZOLL MEDICAL CORP.
K102174	08/02/2010	ZOLL PROPAQ M	ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS
K102468	08/30/2010	ZOLL PROPAQ MD	ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS
K032691	09/02/2003	ZOLL AUTOCLAVABLE INTERNAL HANDLES	ZOLL MEDICAL CORP.
K993036	09/09/1999	ZOLL M SERIES ETCO2 OPTION	ZOLL MEDICAL CORP.
K983538	10/09/1998	MINIATURIZED BIOPSY,SCOPE A.K.A: BIOPSY NEEDLE WITH ENDOSCOPIC VIEWING CAPABILITY	SOLOS ENDOSCOPY, INC.
K033474	11/03/2003	ZOLL AED PLUS	ZOLL MEDICAL CORP.