FDA 510(k) Applications Submitted by DENNIS GRIFFIN

FDA 510(k) Number	Submission Date	Device Name	Applicant
K955435	10/02/1995	ACCESS TOTAL T3 ASSAY (MODIFICATION)	BIO-RAD LABORATORIES, INC.
K955436	10/02/1995	ACCESS VITAMIN B12 ASSAY (MODIFICATION)	BIO-RAD LABORATORIES, INC.
K974560	12/05/1997	CORDIS VANGUARD STEERABLE GUIDEWIRES	CORDIS CORP.
K000715	03/02/2000	ENVOY AND VISTA BRITE TIP	CORDIS CORP.
K960913	03/06/1996	ACCESS FREE T3 ASSAY	BIO-RAD LABORATORIES, INC.
K001135	04/10/2000	6F & 7F INTRODUCING CATHETERS (MODIFICATION)	CORDIS CORP.
K992673	08/10/1999	VISTA BRITE TIP CATHETERS	CORDIS CORP.
K955769	12/21/1995	ACCESS PROGESTERONE ASSAY	BIO-RAD LABORATORIES, INC.
K994358	12/27/1999	ATW MARKER WIRE STEERABLE GUIDEWIRE	CORDIS CORP.