FDA 510(k)

EQ-M

K 號：K210475 · 2022-09-21

決定日期2022-09-21

產品代碼EKX

諮詢委員會DE

決定相當於

器材摘要

EQ-M 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 2022-09-21 under 510(k) number K210475. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

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.

其他以 Meta Systems Co., Ltd. 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

K253461德米專業版 K210789EQ-PEX K153285EMS-200

相關器械（代碼：EKX）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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