EQ-M
K-Number: K210475 · 2022-09-21
Device Summary
Frequently Asked Questions
What is the EQ-M?
EQ-M is a medical device that received FDA 510(k) clearance on 2022-09-21. The listed applicant is Meta Systems Co., Ltd.. The 510(k) number is K210475.
When did EQ-M receive FDA 510(k) clearance?
EQ-M received FDA 510(k) clearance on 2022-09-21, under 510(k) number K210475.
Who is the listed applicant for EQ-M?
The FDA 510(k) record lists Meta Systems Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EQ-M?
The FDA product code for EQ-M is EKX.
Other records listing Meta Systems Co., Ltd. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: EKX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.