FDA 510(k)

Atteris No-Sting Skin Protectant

K 號：K160684 · 2016-07-26

決定日期2016-07-26

產品代碼KMF

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

Atteris No-Sting Skin Protectant is the device name listed in this FDA 510(k) record. The listed applicant is Rochal Industries, LLC. It received FDA 510(k) clearance on 2016-07-26 under 510(k) number K160684. The device is classified under product code KMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Atteris No-Sting Skin Protectant?

Atteris No-Sting Skin Protectant is a medical device that received FDA 510(k) clearance on 2016-07-26. The listed applicant is Rochal Industries, LLC. The 510(k) number is K160684.

When did Atteris No-Sting Skin Protectant receive FDA 510(k) clearance?

Atteris No-Sting Skin Protectant received FDA 510(k) clearance on 2016-07-26, under 510(k) number K160684.

Who is the listed applicant for Atteris No-Sting Skin Protectant?

The FDA 510(k) record lists Rochal Industries, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Atteris No-Sting Skin Protectant?

The FDA product code for Atteris No-Sting Skin Protectant is KMF.

其他以 Rochal Industries, LLC 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：KMF）

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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