FDA 510(k) Applications Submitted by CAROLYN ANDERSON

FDA 510(k) Number	Submission Date	Device Name	Applicant
K040345	02/12/2004	MODIFICATION TO NITREX NITINOL GUIDEWIRE	EV3 INC
K060774	03/22/2006	FOLATE ON THE ACCESS IMMUNOASSAY SYSTEMS, MODEL A14208	BECKMAN COULTER, INC.
K991114	04/01/1999	REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEM	LIFECORE BIOMEDICAL, INC.
K031864	06/16/2003	NITREX NITINOL GUIDEWIRE	EV3 CORPORATION
K002037	07/05/2000	LIFECORE BIOMEDICAL DENTAL IMPLANT SYSTEMS	LIFECORE BIOMEDICAL, INC.
K052082	08/02/2005	FERRITIN ON THE ACCESS IMMUNOASSAY SYSTEMS, MODEL 33020	BECKMAN COULTER, INC.
K003226	10/16/2000	THE LIFECORE STAGE-1 SINGLE STAGE RBM DENTAL IMPLANT SYSTEM	LIFECORE BIOMEDICAL, INC.
K993894	11/16/1999	LIFECORE SINGLE TOOTH ABUTMENT SYSTEM	LIFECORE BIOMEDICAL, INC.
K994205	12/01/1999	MODIFICATION OF REGULAR DIAMETER SINGLE STAGE (RDS) TPS DENTAL IMPLANT SYSTEM	LIFECORE BIOMEDICAL, INC.