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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 the device name listed in this FDA 510(k) record. The listed applicant is Meta Systems Co., Ltd.. It received FDA 510(k) clearance on 2021-10-20 under 510(k) 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. The listed applicant is Meta Systems Co., Ltd.. The 510(k) number is K210789.

When did EQ-PEX receive FDA 510(k) clearance?

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

Who is the listed applicant for EQ-PEX?

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-PEX?

The FDA product code for EQ-PEX is LQY.

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.

K253461Demi ProK210475EQ-MK153285EMS-200

Related Devices (Code: LQY)

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.

K252224Apex Locator (FindPex)Changzhou Sifary Medical Technology Co., Ltd.K242383Apex LocatorShenzhen Rogin Medical Co., Ltd.K242765Electronic Apex Locator (Alpha Apex I)SHENZHEN SUPERLINE TECHNOLOGY CO., LTD.K231990Apex LocatorCefla S.C.K232717Apex Locator (AL-Pex), Apex Locator (AL-Pex+)Changzhou Haili Medical Co., Ltd.K212178Root Apex LocatorFoshan Coxo Medical Instrument Co., Ltd.

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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