Novartis Nutrition Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novartis Nutrition Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Novartis Nutrition Corp. has 5 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 5 cleared submissions from 1998 to 2008. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Novartis Nutrition Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Novartis Nutrition Corp.
5 devices
Cleared
Mar 05, 2008
COMPAT DUALFLO ENTERAL DELIVERY PUMP SET WITH SPIKERIGHT PIERCING SPIKE AND...
Gastroenterology & Urology
26d
Cleared
Jul 23, 2007
NOVARTIS COMPAT SURGICAL GASTROSTOMY JEJUNOSTOMY FEEDING TUBE KIT
Gastroenterology & Urology
84d
Cleared
Feb 16, 2001
COMPAT REPLACEMENT GASTROSTOMY TUBE KIT, MODEL 0974XX
Gastroenterology & Urology
238d
Cleared
Jul 26, 1999
COMPAT JEJUNOSTOMY TUBE KIT, MODEL 088OXX (XX=16,14, OR 12)
Gastroenterology & Urology
73d
Cleared
Oct 09, 1998
COMPAT MINI-G REPLACEMENT GASTROSTOMY TUBE
Gastroenterology & Urology
179d