This page includes the latest FDA filings for Schiff Co. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
Schiff Co holds import registrations or U.S. agent authorizations in conjunction with the following organizations:
Device Company | Device | Date |
|---|---|---|
SCHIFF & CO. | X-TIP INTRAOSSEOUS PERFORATOR | 1999-04-27 |
SCHIFF & CO. | JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200 | 1999-03-24 |
SCHIFF & CO. | NUTRISAFE ENTERAL FEEDING TUBE | 1999-02-04 |
SCHIFF & CO. | VYGON DOUBLE LUMEN UMBILICAL CATHETER | 1998-10-01 |
SCHIFF & CO. | PLUS REUSABLE RESUSCITATOR | 1998-05-21 |
SCHIFF & CO. | VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM | 1996-10-28 |
SCHIFF & CO. | HM-CAP EIA TEST (MODIFICATION) | 1996-02-09 |
SCHIFF & CO. | HM-CAP EIA KIT | 1995-07-18 |
SCHIFF & CO. | VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE | 1995-02-14 |
SCHIFF & CO. | KEMBLE LIQUID HANDLING SYSTEM DISPENSER | 1990-04-16 |
SCHIFF & CO. | OLYMPUS PK-TP SYSTEM REACTIVE CONTROL | 1989-10-31 |
SCHIFF & CO. | FASTEC 901 AGGLUTINATION PATTERN READER | 1989-10-30 |
SCHIFF & CO. | CLEANTECH SYSTEM | 1988-08-08 |
SCHIFF & CO. | REVISED IMMUDIA HEM-SP | 1988-05-13 |
SCHIFF & CO. | BETA-HCG ASSAY | 1988-02-02 |
SCHIFF AND CO | 0000-00-00 00:00:00 |