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FDA 510(k) Applications Submitted by ANNE MARIE CESARIO, R.A.C.
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.
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