Schiff & Co. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Schiff & Co. has 15 FDA 510(k) cleared medical devices. Based in West Cadwell, US.
Historical record: 15 cleared submissions from 1988 to 1999.
Browse the FDA 510(k) cleared devices submitted by Schiff & Co. Filter by specialty or product code using the sidebar.
15 devices
Cleared
Apr 27, 1999
X-TIP INTRAOSSEOUS PERFORATOR
Dental
68d
Cleared
Mar 24, 1999
JOSTRA VENOUS HARDSHELL CARDIOTOMIC RESERVOIR VHK 4200
Cardiovascular
280d
Cleared
Feb 04, 1999
NUTRISAFE ENTERAL FEEDING TUBE
Gastroenterology & Urology
273d
Cleared
Oct 01, 1998
VYGON DOUBLE LUMEN UMBILICAL CATHETER
General Hospital
147d
Cleared
May 21, 1998
PLUS REUSABLE RESUSCITATOR
Anesthesiology
199d
Cleared
Oct 28, 1996
VIOTEC V-2200 ULTRAVIOLET GERMICIDAL AIR PURIFICATION SYSTEM
General Hospital
399d
Cleared
Feb 09, 1996
HM-CAP EIA TEST (MODIFICATION)
Microbiology
106d
Cleared
Jul 18, 1995
HM-CAP EIA KIT
Microbiology
326d
Cleared
Feb 14, 1995
VIOTEC 1400 SERIES ULTRAVIOLET GERMICIDAL FIXTURE
General Hospital
209d
Cleared
Apr 16, 1990
KEMBLE LIQUID HANDLING SYSTEM DISPENSER
Chemistry
139d
Cleared
Oct 31, 1989
OLYMPUS PK-TP SYSTEM REACTIVE CONTROL
Microbiology
103d
Cleared
Oct 30, 1989
FASTEC 901 AGGLUTINATION PATTERN READER
Microbiology
18d