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FDA 510(k)

潤滑性

K 號:K163476 · 2017-05-10

決定日期2017-05-10
產品代碼LFD
決定相當於

器材摘要

Lubricity is the device name listed in this FDA 510(k) record. The listed applicant is You First Services, Incorporated. It received FDA 510(k) clearance on 2017-05-10 under 510(k) number K163476. The device is classified under product code LFD. FDA Decision: Substantially Equivalent.

常見問題

What is the Lubricity?

Lubricity is a medical device that received FDA 510(k) clearance on 2017-05-10. The listed applicant is You First Services, Incorporated. The 510(k) number is K163476.

When did Lubricity receive FDA 510(k) clearance?

Lubricity received FDA 510(k) clearance on 2017-05-10, under 510(k) number K163476.

Who is the listed applicant for Lubricity?

The FDA 510(k) record lists You First Services, Incorporated as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Lubricity?

The FDA product code for Lubricity is LFD.

相關臨床試驗

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相關器械(代碼:LFD)

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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