Moss Medical Products is one of 15128 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
Recent clearances: Y2K2 ENTERNAL TUBE FLUID FILTER
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.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
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