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FDA 510(k)

REST EAZY 裝置

K 號:K172760 · 2018-03-26

決定日期2018-03-26
產品代碼LRK
諮詢委員會DE
決定相當於

器材摘要

REST EAZY Appliance is the device name listed in this FDA 510(k) record. The listed applicant is Insert Molding Solutions, Inc.. It received FDA 510(k) clearance on 2018-03-26 under 510(k) number K172760. The device is classified under product code LRK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the REST EAZY Appliance?

REST EAZY Appliance is a medical device that received FDA 510(k) clearance on 2018-03-26. The listed applicant is Insert Molding Solutions, Inc.. The 510(k) number is K172760.

When did REST EAZY Appliance receive FDA 510(k) clearance?

REST EAZY Appliance received FDA 510(k) clearance on 2018-03-26, under 510(k) number K172760.

Who is the listed applicant for REST EAZY Appliance?

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

What is the FDA product code for REST EAZY Appliance?

The FDA product code for REST EAZY Appliance is LRK.

相關臨床試驗

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相關器械(代碼:LRK)

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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