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FDA 510(k)

舒適普

K 號:K212438 · 2021-12-07

決定日期2021-12-07
產品代碼LYY
諮詢委員會醫療設備規範文本翻譯如下: HO 注意:原文中未提供具體的醫療設備規範文本,因此上述翻譯僅為示例。請提供完整的規範文本以便進行準確翻譯。
決定相當於

器材摘要

Comfortpro is the device name listed in this FDA 510(k) record. The listed applicant is Thai Rubber Industry Company Limited. It received FDA 510(k) clearance on 2021-12-07 under 510(k) number K212438. The device is classified under product code LYY. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Comfortpro?

Comfortpro is a medical device that received FDA 510(k) clearance on 2021-12-07. The listed applicant is Thai Rubber Industry Company Limited. The 510(k) number is K212438.

When did Comfortpro receive FDA 510(k) clearance?

Comfortpro received FDA 510(k) clearance on 2021-12-07, under 510(k) number K212438.

Who is the listed applicant for Comfortpro?

The FDA 510(k) record lists Thai Rubber Industry Company Limited as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Comfortpro?

The FDA product code for Comfortpro is LYY.

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其他以 Thai Rubber Industry Company Limited 為申請人之記錄

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相關器械(代碼:LYY)

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。

官方來源

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