EsophyX Z+ Device with SerosaFuse Fasteners and Accessories
K-Number: K240879 · 2024-04-26
Device Summary
Frequently Asked Questions
What is the EsophyX Z+ Device with SerosaFuse Fasteners and Accessories?
EsophyX Z+ Device with SerosaFuse Fasteners and Accessories is a medical device that received FDA 510(k) clearance on 2024-04-26. It is manufactured by Endogastric Solutions, Inc.. The 510(k) number is K240879.
When was EsophyX Z+ Device with SerosaFuse Fasteners and Accessories approved by the FDA?
EsophyX Z+ Device with SerosaFuse Fasteners and Accessories received FDA 510(k) clearance on 2024-04-26, under approval number K240879.
What company makes EsophyX Z+ Device with SerosaFuse Fasteners and Accessories?
EsophyX Z+ Device with SerosaFuse Fasteners and Accessories is manufactured by Endogastric Solutions, Inc..
What is the FDA product code for EsophyX Z+ Device with SerosaFuse Fasteners and Accessories?
The FDA product code for EsophyX Z+ Device with SerosaFuse Fasteners and Accessories is ODE.
Other Devices by Endogastric Solutions, Inc.
Related Devices (Code: ODE)
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.