FDA 510(k)

複合W氮氫冷凍劑

K 號：K172373 · 2017-11-02

決定日期2017-11-02

產品代碼GEH

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

Compound W Nitro-Freeze is the device name listed in this FDA 510(k) record. The listed applicant is Medtech Products, Inc.. It received FDA 510(k) clearance on 2017-11-02 under 510(k) number K172373. The device is classified under product code GEH. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Compound W Nitro-Freeze?

Compound W Nitro-Freeze is a medical device that received FDA 510(k) clearance on 2017-11-02. The listed applicant is Medtech Products, Inc.. The 510(k) number is K172373.

When did Compound W Nitro-Freeze receive FDA 510(k) clearance?

Compound W Nitro-Freeze received FDA 510(k) clearance on 2017-11-02, under 510(k) number K172373.

Who is the listed applicant for Compound W Nitro-Freeze?

The FDA 510(k) record lists Medtech Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Compound W Nitro-Freeze?

The FDA product code for Compound W Nitro-Freeze is GEH.

其他以 Medtech Products, Inc. 為申請人之記錄

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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相關器械（代碼：GEH）

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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