FDA 510(k)

LS 油脂

K 號：K173920 · 2018-10-11

決定日期2018-10-11

產品代碼EKX

諮詢委員會DE

決定相當於

器材摘要

LS OIL is the device name listed in this FDA 510(k) record. The listed applicant is J. Morita USA, Inc.. It received FDA 510(k) clearance on 2018-10-11 under 510(k) number K173920. The device is classified under product code EKX. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the LS OIL?

LS OIL is a medical device that received FDA 510(k) clearance on 2018-10-11. The listed applicant is J. Morita USA, Inc.. The 510(k) number is K173920.

When did LS OIL receive FDA 510(k) clearance?

LS OIL received FDA 510(k) clearance on 2018-10-11, under 510(k) number K173920.

Who is the listed applicant for LS OIL?

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

What is the FDA product code for LS OIL?

The FDA product code for LS OIL is EKX.

其他以 J. Morita USA, Inc. 為申請人之記錄

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相關器械（代碼：EKX）

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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