FDA 510(k) Applications Submitted by SCHILLER AG

FDA 510(k) Number	Submission Date	Device Name	Applicant
K221056	04/11/2022	ARGUS PB-3000	SCHILLER 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
K063814	12/22/2006	BP-200 PLUS	SCHILLER AG
K183425	12/11/2018	CARDIOVIT AT-102 G2	Schiller AG
K101619	06/09/2010	WELCH ALLYN 1500 PATIENT MONITOR	SCHILLER AG
K170182	01/23/2017	CARDIOVIT FT-1	SCHILLER AG
K152043	07/23/2015	Diagnostic Station DS20	SCHILLER AG