AquaShield System - PENTAX, AquaShield System CO2 - PENTAX, AquaShield System CO2 - FUJINON
Jan 2017
29d
United State Endoscopy Group, Inc. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
United State Endoscopy Group, Inc. has 1 FDA 510(k) cleared medical devices. Based in Mentor, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by United State Endoscopy Group, Inc. Filter by specialty or product code using the sidebar.
1 devices