FDA 510(k) Applications Submitted by MARKUS BUETLER

FDA 510(k) Number	Submission Date	Device Name	Applicant
K130210	01/29/2013	MEDELA THOPAZ	MEDELA AG
K050686	03/16/2005	CARDIOVIT AT-10PLUS	SCHILLER AG
K031557	05/19/2003	CARDIOVIT AT-102	SCHILLER AG
K051368	05/25/2005	BR 102 PLUS BLOOD PRESSURE HOLTER SYSTEM	SCHILLER AG
K012226	07/16/2001	MONITORING SYSTEM,MODEL ARGUS PB-1000	SCHILLER AG
K992823	08/23/1999	SPIROVIT SP-2, PNEUMOCHECK II	SCHILLER AG
K984031	11/12/1998	SPIROVIT, MODEL SP-250	SCHILLER AG
K053207	11/16/2005	ARGUS, MODEL LCM	SCHILLER AG
K033738	11/28/2003	MONITORING SYSTEM, MODEL ARGUS PB-2200	SCHILLER AG