FDA 510(k) Applications Submitted by ANNE M CESARIO

FDA 510(k) Number	Submission Date	Device Name	Applicant
K964702	11/25/1996	EUCLID SYSTEMS CORNEAL TOPOGRAPHER MODEL ET800	EUCLID SYSTEMS CORP.
K981629	05/07/1998	NUTRISAFE ENTERAL FEEDING TUBE	SCHIFF & CO.
K981630	05/07/1998	VYGON DOUBLE LUMEN UMBILICAL CATHETER	SCHIFF & CO.
K982136	06/17/1998	JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200	SCHIFF & CO.
K974141	11/03/1997	PLUS REUSABLE RESUSCITATOR	SCHIFF & CO.
K960541	02/07/1996	LYNX DPA DISPOSABLE PROPHY ANGLE	MTI PRECISION PRODUCTS
K960795	02/27/1996	VYGON DOUBLE LUMEN ENDOTRACHEAL TUBE	VYGON CORP.
K960833	02/29/1996	VIOTEC S-4000-CR SECURITY SERIES ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM	UV TECHNOLOGIES, INC.
K963195	08/15/1996	WIRELESS EEG RECORDING SYSTEM MODEL W32	CME TELEMETRIX, INC.
K963196	08/15/1996	VYGON UMBILICAL CATHETHER INSERTION TRAY	VYGON CORP.
K963373	08/27/1996	COSMED K4	COSMED S.R.L.
K963571	09/05/1996	VYGON MULTI-DOSE VIAL ADAPTER & BIONECTOR	VYGON CORP.
K954448	09/25/1995	VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM	SCHIFF & CO.
K963981	10/03/1996	VYGON BIONECTOR WITH EXTENSION SET	VYGON CORP.
K954638	10/06/1995	5 FR PICC-LINE CATHETER	VYGON CORP.
K974806	12/23/1997	VYGON NEO-SUMP	VYGON CORP.
K983544	10/09/1998	VYGON DOUBLE LUMEN PICC-CATHETERS (4FR. AND 5FR.)	VYGON CORP.