Canada Endoscope Corporation is one of 461 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Canada Endoscope Corporation - FDA 510(k) Cleared Devices
Recent clearances: CYSTOSCOPE, MODELS CE0004-C, CE006-C, CE3004-C, CE3027-C, CE7004-C, CE1204-C, CE1227-C
1
Total
1
Cleared
0
Denied
Canada Endoscope Corporation has 1 FDA 510(k) cleared medical devices. Based in Pickering, On, CA.
Historical record: 1 cleared submissions from 2010 to 2010. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Canada Endoscope Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Canada Endoscope Corporation
1 devices