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FDA 510(k)

FORA MD6 開放性鹽酸監測系統，FORA MD6 Pro 開放性鹽酸監測系統

K 號：K181675 · 2018-12-10

申請人Taidoc Technology Corporation
決定日期2018-12-10
產品代碼PTC
諮詢委員會CH
決定相當於

器材摘要

FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid 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 2018-12-10 under 510(k) number K181675. The device is classified under product code PTC. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System?

FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System is a medical device that received FDA 510(k) clearance on 2018-12-10. The listed applicant is Taidoc Technology Corporation. The 510(k) number is K181675.

When did FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System receive FDA 510(k) clearance?

FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System received FDA 510(k) clearance on 2018-12-10, under 510(k) number K181675.

Who is the listed applicant for FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid 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 MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System?

The FDA product code for FORA MD6 Uric Acid Monitoring System, FORA MD6 Pro Uric Acid Monitoring System is PTC.

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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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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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