FDA 510(k) Applications Submitted by STOCKERT INSTRUMENTE GMBH

FDA 510(k) Number	Submission Date	Device Name	Applicant
K020571	02/21/2002	STOCKERT CENTRIFUGAL PUMP CONSOLE	STOCKERT INSTRUMENTE GMBH
K032213	07/21/2003	STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP	STOCKERT INSTRUMENTE GMBH
K022280	07/15/2002	STOCKERT CORONARY PERFUSION CANNULAE	STOCKERT INSTRUMENTE GMBH
K023622	10/29/2002	STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-35	STOCKERT INSTRUMENTE GMBH
K011088	04/10/2001	SIII ALARM AMPLIFIER	STOCKERT INSTRUMENTE GMBH
K041558	06/10/2004	STOCKERTIR PURGE CONTROL (APC) SYSTEM	STOCKERT INSTRUMENTE GMBH
K011838	06/12/2001	CENTRIFUGAL PUMP	STOCKERT INSTRUMENTE GMBH
K042374	09/01/2004	STOCKERT SCP RHYTHM	STOCKERT INSTRUMENTE GMBH
K022321	07/17/2002	STOCKERT V172-28 VENOUS FEMORAL CANNULA	STOCKERT INSTRUMENTE GMBH