EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil
K-Number: K232126 · 2023-08-16
Device Summary
Frequently Asked Questions
What is the EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil?
EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil is a medical device that received FDA 510(k) clearance on 2023-08-16. It is manufactured by Covidien. The 510(k) number is K232126.
When was EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil approved by the FDA?
EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil received FDA 510(k) clearance on 2023-08-16, under approval number K232126.
What company makes EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil?
EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil is manufactured by Covidien.
What is the FDA product code for EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil?
The FDA product code for EEACircular Stapler with Tri-Staple Technology and OrVil Transoral Circular Stapler Anvil is GAG.
Related Clinical Trials
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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.