FDA 510(k)

MD-Temp Plus

K 號：K190724 · 2019-07-03

決定日期2019-07-03

產品代碼EBG

諮詢委員會DE

決定相當於

器材摘要

MD-Temp Plus is the device name listed in this FDA 510(k) record. The listed applicant is Meta Biomed Co., Ltd.. It received FDA 510(k) clearance on 2019-07-03 under 510(k) number K190724. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MD-Temp Plus?

MD-Temp Plus is a medical device that received FDA 510(k) clearance on 2019-07-03. The listed applicant is Meta Biomed Co., Ltd.. The 510(k) number is K190724.

When did MD-Temp Plus receive FDA 510(k) clearance?

MD-Temp Plus received FDA 510(k) clearance on 2019-07-03, under 510(k) number K190724.

Who is the listed applicant for MD-Temp Plus?

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

What is the FDA product code for MD-Temp Plus?

The FDA product code for MD-Temp Plus is EBG.

其他以 Meta Biomed Co., Ltd. 為申請人之記錄

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相關器械（代碼：EBG）

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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