EQ-M
K-Number: K210475 · 2022-09-21
ApplicantMeta Systems Co., Ltd.
Decision Date2022-09-21
Product CodeEKX
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
EQ-M is a medical device manufactured by Meta Systems Co., Ltd.. It received FDA 510(k) clearance on 2022-09-21 under approval number K210475. 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 EQ-M?
EQ-M is a medical device that received FDA 510(k) clearance on 2022-09-21. It is manufactured by Meta Systems Co., Ltd.. The 510(k) number is K210475.
When was EQ-M approved by the FDA?
EQ-M received FDA 510(k) clearance on 2022-09-21, under approval number K210475.
What company makes EQ-M?
EQ-M is manufactured by Meta Systems Co., Ltd..
What is the FDA product code for EQ-M?
The FDA product code for EQ-M is EKX.
Other Devices by Meta Systems 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.