Moss Medical Products is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Moss Medical Products - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Moss Medical Products has 8 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 8 cleared submissions from 1991 to 2005. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Moss Medical Products Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Moss Medical Products
8 devices
Cleared
Nov 02, 2005
Y2K2 ENTERNAL TUBE FLUID FILTER
Gastroenterology & Urology
175d
Cleared
May 11, 2004
Y2K2 ENTERNAL FEEDING MANAGER
Gastroenterology & Urology
459d
Cleared
Feb 05, 2004
MOSSMED DUAL INTERMITTENT ASPIRATOR
Gastroenterology & Urology
269d
Cleared
Feb 14, 1992
MOSS - ANCHOR SET
Gastroenterology & Urology
179d
Cleared
Jun 24, 1991
MOSS- ANCHOR SET
Gastroenterology & Urology
111d
Cleared
May 28, 1991
MOSS NASAL TUBE MARK IV
Gastroenterology & Urology
84d
Cleared
May 03, 1991
MOSS P.E.G. TRAY
Gastroenterology & Urology
59d
Cleared
Apr 19, 1991
MOSS GASTROSTOMY TUBE
Gastroenterology & Urology
45d