FDA 510(k)

Sleepio®

K 號：K233577 · 2024-08-05

決定日期2024-08-05

產品代碼QVO

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

Sleepio® is the device name listed in this FDA 510(k) record. The listed applicant is Big Health, Inc.. It received FDA 510(k) clearance on 2024-08-05 under 510(k) number K233577. The device is classified under product code QVO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Sleepio®?

Sleepio® is a medical device that received FDA 510(k) clearance on 2024-08-05. The listed applicant is Big Health, Inc.. The 510(k) number is K233577.

When did Sleepio® receive FDA 510(k) clearance?

Sleepio® received FDA 510(k) clearance on 2024-08-05, under 510(k) number K233577.

Who is the listed applicant for Sleepio®?

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

What is the FDA product code for Sleepio®?

The FDA product code for Sleepio® is QVO.

其他以 Big Health, Inc. 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。

K233872Daylight

相關器械（代碼：QVO）

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。

K191716某麥斯特Pear Therapeutics, Inc.

官方來源

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