AquaShield System CO2- Fujifilm
K-Number: K173650 · 2018-01-05
Device Summary
Frequently Asked Questions
What is the AquaShield System CO2- Fujifilm?
AquaShield System CO2- Fujifilm is a medical device that received FDA 510(k) clearance on 2018-01-05. It is manufactured by United States Endoscopy Group, Inc.. The 510(k) number is K173650.
When was AquaShield System CO2- Fujifilm approved by the FDA?
AquaShield System CO2- Fujifilm received FDA 510(k) clearance on 2018-01-05, under approval number K173650.
What company makes AquaShield System CO2- Fujifilm?
AquaShield System CO2- Fujifilm is manufactured by United States Endoscopy Group, Inc..
What is the FDA product code for AquaShield System CO2- Fujifilm?
The FDA product code for AquaShield System CO2- Fujifilm is FEQ.
Other Devices by United States Endoscopy Group, Inc.
Related Devices (Code: FEQ)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.