Endo Motor
K-Number: K220829 · 2023-05-18
Decision Date2023-05-18
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Endo Motor is a medical device manufactured by Foshan Coxo Medical Instrument Co., Ltd.. It received FDA 510(k) clearance on 2023-05-18 under approval number K220829. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Endo Motor?
Endo Motor is a medical device that received FDA 510(k) clearance on 2023-05-18. It is manufactured by Foshan Coxo Medical Instrument Co., Ltd.. The 510(k) number is K220829.
When was Endo Motor approved by the FDA?
Endo Motor received FDA 510(k) clearance on 2023-05-18, under approval number K220829.
What company makes Endo Motor?
Endo Motor is manufactured by Foshan Coxo Medical Instrument Co., Ltd..
What is the FDA product code for Endo Motor?
The FDA product code for Endo Motor is EKX.
Other Devices by Foshan Coxo Medical Instrument Co., Ltd.
Related Devices (Code: EKX)
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.