FDA 510(k)

DT-703

K 號：K221233 · 2022-06-27

決定日期2022-06-27

產品代碼EHD

諮詢委員會DE

決定相當於

器材摘要

DT-703 is the device name listed in this FDA 510(k) record. The listed applicant is Ecotron Co., Ltd.. It received FDA 510(k) clearance on 2022-06-27 under 510(k) number K221233. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the DT-703?

DT-703 is a medical device that received FDA 510(k) clearance on 2022-06-27. The listed applicant is Ecotron Co., Ltd.. The 510(k) number is K221233.

When did DT-703 receive FDA 510(k) clearance?

DT-703 received FDA 510(k) clearance on 2022-06-27, under 510(k) number K221233.

Who is the listed applicant for DT-703?

The FDA 510(k) record lists Ecotron Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DT-703?

The FDA product code for DT-703 is EHD.

其他以 Ecotron Co., Ltd. 為申請人之記錄

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