FDA 510(k)

FORA先進GD40血糖、β-酮體及膽固醇監測系統

K 號：K201037 · 2022-06-16

決定日期2022-06-16

產品代碼NBW

諮詢委員會CH

決定相當於

器材摘要

FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System is the device name listed in this FDA 510(k) record. The listed applicant is Taidoc Technology Corporation. It received FDA 510(k) clearance on 2022-06-16 under 510(k) number K201037. The device is classified under product code NBW. It was reviewed by the CH advisory panel. Product code NBW falls under the category of OB/GYN, which includes obstetric and gynecological diagnostic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

常見問題

What is the FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System?

FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System is a medical device that received FDA 510(k) clearance on 2022-06-16. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K201037.

When did FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System receive FDA 510(k) clearance?

FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System received FDA 510(k) clearance on 2022-06-16, under 510(k) number K201037.

Who is the listed applicant for FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System?

The FDA 510(k) record lists Taidoc Technology Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System?

The FDA product code for FORA ADVANCED GD40 Glucose, ß-Ketone and Cholesterol Monitoring System is NBW. This falls under the OB/GYN category.

其他以 Taidoc Technology Corporation 為申請人之記錄

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相關器械（代碼：NBW）

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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