FDA 510(k) Applications Submitted by JOHN G D'ANGELO

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020374	02/04/2002	OCULIGHT SL/SLX	IRIDEX CORP.
K020849	03/15/2002	APEX 800 LASER SYSTEM, MODEL APEX 800	IRIDEX CORP.
K981266	04/07/1998	AUTO-INJECTOR, SURE-INJECT 2000	MIGHTY MO, CORP.
K022228	07/10/2002	FAMILY OF IRIS MEDICAL ENDOPROBE HANDPIECES	IRIDEX CORP.
K982816	08/11/1998	VNUS CLOSURE SYSTEM	VNUS MEDICAL TECHNOLOGIES, INC.
K082562	09/04/2008	APPLIED BIOSYSTEMS 7500 FAST DX	APPLIED BIOSYSTEMS INC
K993900	11/16/1999	COAGULATION ELECTRODE, MODEL 2000; RADIOFREQUENCY GENERATOR, MODEL 20-115	BRONCUS TECHNOLOGIES, INC.
K955594	12/08/1995	SAFELINE I.V. BAG ACCESS DEVICE	MCGAW, INC.
K955595	12/08/1995	SAFELINE MULTIDOSE VIAL ADAPTER	MCGAW, INC.