FDA 510(k) Applications Submitted by VICKI DREWS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K002739	09/01/2000	INFUSOR PATIENT CONTROL MODULE, 2ML, MODEL 2C1067K	BAXTER HEALTHCARE CORP.
K011317	04/30/2001	MULTIRATE INFUSOR SV; MULTIRATE INFUSER LV; BAXTER PAIN MATE PAIN MANAGEMENT SYSTEM	BAXTER HEALTHCARE CORP.
K982102	06/15/1998	SINGLEDAY INFUSOR 2 ML/HR (ELASTOMERIC INFUSION DEVICE) MODEL, INFUSOR SV 5 ML/HR (ELASTOMERIC INFUSION DEVICE) MODEL CY	BAXTER HEALTHCARE CORP.
K002380	08/04/2000	INFUSOR SV, INFUSOR LV, BAXTER PAIN MANAGEMENT SYSTEM	BAXTER HEALTHCARE CORP.
K993387	10/08/1999	IPUMP PAIN MANAGEMENT SYSTEM, MODEL 2L3107K	BAXTER HEALTHCARE CORP.