Easyglide , Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Easyglide , Ltd. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Easyglide , Ltd. has 5 FDA 510(k) cleared medical devices. Based in Bonita Springs, US.
Historical record: 5 cleared submissions from 2009 to 2012. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Easyglide , Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Easyglide , Ltd.
5 devices
Cleared
May 16, 2012
CLEARPATH LOWER GI
Gastroenterology & Urology
216d
Cleared
May 16, 2012
CLEARPATH UPPER GI
Gastroenterology & Urology
202d
Cleared
May 17, 2010
CLEARJET
Gastroenterology & Urology
27d
Cleared
Mar 09, 2010
CLEARPATH UGI
Gastroenterology & Urology
90d
Cleared
Oct 23, 2009
CLEARPATH
Gastroenterology & Urology
172d