FDA 510(k) Applications Submitted by PHOENIX BIOMEDICAL CORP.

FDA 510(k) Number	Submission Date	Device Name	Applicant
K990256	01/27/1999	CRX WORLD SHUNT	PHOENIX BIOMEDICAL CORP.
K030468	02/12/2003	ACURA ELITE GRAVITY COMPENSATING RESERVOIR	PHOENIX BIOMEDICAL CORP.
K000514	02/16/2000	RUMBAR DRAINAGE SYSTEM	PHOENIX BIOMEDICAL CORP.
K991429	04/26/1999	DIAMOND II VALVE	PHOENIX BIOMEDICAL CORP.
K021644	05/20/2002	PERF (OMMAYA STYLE) RESERVOIRS	PHOENIX BIOMEDICAL CORP.
K002476	08/11/2000	LUMBOPERITONEAL SHUNT SYSTEM	PHOENIX BIOMEDICAL CORP.
K024040	12/06/2002	ACCURA ELITE SHUNT SYSTEM	PHOENIX BIOMEDICAL CORP.
K024101	12/12/2002	PHOENIX UNIVERSAL SHUNT SYSTEM	PHOENIX BIOMEDICAL CORP.
K974096	10/30/1997	CRX DIAMOND VALVE	PHOENIX BIOMEDICAL CORP.
K960435	01/31/1996	PHOENIX CRX VALVE	PHOENIX BIOMEDICAL CORP.
K962144	06/03/1996	PHOENIX ETE TISSUE EXTENSION SYSTEM	PHOENIX BIOMEDICAL CORP.
K953128	07/06/1995	SUTURE CORD	PHOENIX BIOMEDICAL CORP.