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FDA 510(k)

EQ-PEX

K-Number: K210789 · 2021-10-20

ApplicantMeta Systems Co., Ltd.
Decision Date2021-10-20
Product CodeLQY
DecisionSubstantially Equivalent

Device Summary

EQ-PEX is a medical device manufactured by Meta Systems Co., Ltd.. It received FDA 510(k) clearance on 2021-10-20 under approval number K210789. The device is classified under product code LQY. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EQ-PEX?

EQ-PEX is a medical device that received FDA 510(k) clearance on 2021-10-20. It is manufactured by Meta Systems Co., Ltd.. The 510(k) number is K210789.

When was EQ-PEX approved by the FDA?

EQ-PEX received FDA 510(k) clearance on 2021-10-20, under approval number K210789.

What company makes EQ-PEX?

EQ-PEX is manufactured by Meta Systems Co., Ltd..

What is the FDA product code for EQ-PEX?

The FDA product code for EQ-PEX is LQY.

Other Devices by Meta Systems Co., Ltd.

K153285EMS-200 K210475EQ-M K253461Demi Pro

Related Devices (Code: LQY)

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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.

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