FDA 510(k) Applications Submitted by RICHARD D BLISS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K002813	09/08/2000	NIPRO SAFETOUCH SAFETY FISTULA NEEDLE	NIPRO MEDICAL CORP.
K032777	09/08/2003	MODIFICATION TO: NIPRO SAFE TOUCH SAFETY FISTULA NEEDLE	NIPRO MEDICAL CORP.
K023007	09/09/2002	DISTAL RADIUS FRACTURE REPAIR SYSTEM	HAND INNOVATIONS, INC.
K010264	01/29/2001	NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SET	NIPRO MEDICAL CORP.
K030198	01/21/2003	HAND INNOVATIONS, INC. DISTAL RADIUS FRACTURE REPAIR SYSTEM	HAND INNOVATIONS, INC.
K981622	05/07/1998	DADE TRU-LIQUID CARDIAC CONTROL	DADE BEHRING, INC.
K001465	05/10/2000	NIPRO BLOOD TUBING SET FOR HEMODIALYSIS WITH TRANSDUCER PROTECTORS AND PRIMING SET	NIPRO MEDICAL CORP.