Ross Product Div. Abbott Laboratories - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Ross Product Div. Abbott Laboratories has 4 FDA 510(k) cleared medical devices. Based in Columbus, US.
Historical record: 4 cleared submissions from 1999 to 2003. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Ross Product Div. Abbott Laboratories Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Ross Product Div. Abbott Laboratories
4 devices
Cleared
May 20, 2003
ROSS EMBRACE ENTERAL PUMP
General Hospital
15d
Cleared
Jun 12, 2001
AMBULATORY ENTERAL NUTRITION PUMP
General Hospital
256d
Cleared
Aug 25, 1999
FLEXIFLO ENTERAL FEEDING TUBE
Gastroenterology & Urology
30d
Cleared
Apr 06, 1999
MODIFICATION TO FLEXFLO POLYG GASTROSTOMY TUBE
Gastroenterology & Urology
21d