Mpathy Medical Devices, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Mpathy Medical Devices, Ltd. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Mpathy Medical Devices, Ltd. has 6 FDA 510(k) cleared medical devices. Based in Fairfield, US.
Historical record: 6 cleared submissions from 2004 to 2009. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Mpathy Medical Devices, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Mpathy Medical Devices, Ltd.
6 devices
Cleared
Aug 12, 2009
OMNISURE URETHRAL SLING, MODEL OTK52
Gastroenterology & Urology
21d
Cleared
Jul 14, 2009
MINITAPE URETHRAL SLING
Gastroenterology & Urology
82d
Cleared
Mar 03, 2008
MINITAPE EXTRA URETHRAL SLING
Gastroenterology & Urology
68d
Cleared
Feb 25, 2008
MINITAPE URETHRAL SLING
Gastroenterology & Urology
61d
Cleared
Feb 06, 2006
MODIFICATION TO: MINIMESH POLYPROPYLENE MESH
Obstetrics & Gynecology
66d
Cleared
Nov 17, 2004
MINIMESH POLYPROPYLENE MESH
Obstetrics & Gynecology
154d