FDA 510(k) Applications Submitted by ROBERT D WAXHAM

FDA 510(k) Number	Submission Date	Device Name	Applicant
K000675	02/28/2000	MANUAL DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-502	JAWON MEDICAL CO., LTD.
K981702	05/14/1998	AUTOMATIC DIGITAL ELECTRONIC WRIST BLOOD PRESSURE MONITOR MODEL NUMBER WS-300	NIHON SEIMITSU SOKKI CO., LTD.
K991688	05/17/1999	WRIST TYPE DIGITAL BLOOD PRESSURE MONITOR, MODEL HD-303S	JAWON MEDICAL CO., LTD.
K003444	11/06/2000	MODEL WS-500 DIGITAL WRIST BLOOD PRESSURE MONITOR	NIHON SEIMITSU SOKKI CO., LTD.
K993890	11/16/1999	DIGITAL BLOOD PRESSURE MONITOR, MODEL DS-181	NIHON SEIMITSU SOKKI CO., LTD.