FDA 510(k) Applications Submitted by DAVID TUCKER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K002650	08/25/2000	VAN ANDLE DILATION, EMERALD GUIDEWIRE, MODEL VAD6, 502-726	BENTEC MEDICAL, INC.
K991291	04/15/1999	STRETTA INFLATABLE BASKET CATHETER ELECTRODE WITH ASPIRATION	CONWAY STUART MEDICAL, INC.
K991529	05/03/1999	CSM STRETTA CONTROL MODULE ELECTROSURGICAL GENERATOR, MODEL S400	CONWAY STUART MEDICAL, INC.
K983871	11/02/1998	RITA MODEL 70 ELECTROSURGICAL PROBE	RITA MEDICAL SYSTEMS
K955121	11/09/1995	HEARTPORT ENDOARTERIAL RETURN CANNUAL	HEARTPORT, INC.
K955132	11/09/1995	HEARTPORT ENDOAORTIC CLAMP	HEARTPORT, INC.