AtriClip FLEX-Mini LAA Exclusion System (ACHM)
K-Number: K234125 · 2024-07-29
Device Summary
Frequently Asked Questions
What is the AtriClip FLEX-Mini LAA Exclusion System (ACHM)?
AtriClip FLEX-Mini LAA Exclusion System (ACHM) is a medical device that received FDA 510(k) clearance on 2024-07-29. It is manufactured by AtriCure, Inc.. The 510(k) number is K234125.
When was AtriClip FLEX-Mini LAA Exclusion System (ACHM) approved by the FDA?
AtriClip FLEX-Mini LAA Exclusion System (ACHM) received FDA 510(k) clearance on 2024-07-29, under approval number K234125.
What company makes AtriClip FLEX-Mini LAA Exclusion System (ACHM)?
AtriClip FLEX-Mini LAA Exclusion System (ACHM) is manufactured by AtriCure, Inc..
What is the FDA product code for AtriClip FLEX-Mini LAA Exclusion System (ACHM)?
The FDA product code for AtriClip FLEX-Mini LAA Exclusion System (ACHM) is PZX.
Related Clinical Trials
Other Devices by AtriCure, Inc.
Related Devices (Code: PZX)
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.