FDA 510(k)

Elevo® 噪鼾干預設備

K 號：K181107 · 2018-12-06

決定日期2018-12-06

產品代碼LRK

諮詢委員會DE

決定相當於

器材摘要

Elevo® Kit Snoring Intervention Device is the device name listed in this FDA 510(k) record. The listed applicant is Zelegent, Inc.. It received FDA 510(k) clearance on 2018-12-06 under 510(k) number K181107. 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 Elevo® Kit Snoring Intervention Device?

Elevo® Kit Snoring Intervention Device is a medical device that received FDA 510(k) clearance on 2018-12-06. The listed applicant is Zelegent, Inc.. The 510(k) number is K181107.

When did Elevo® Kit Snoring Intervention Device receive FDA 510(k) clearance?

Elevo® Kit Snoring Intervention Device received FDA 510(k) clearance on 2018-12-06, under 510(k) number K181107.

Who is the listed applicant for Elevo® Kit Snoring Intervention Device?

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

What is the FDA product code for Elevo® Kit Snoring Intervention Device?

The FDA product code for Elevo® Kit Snoring Intervention Device is LRK.

其他以 Zelegent, Inc. 為申請人之記錄

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K213475Elevo鼾症介入組合

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。

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