Daylight
K 號：K233872 · 2024-08-30
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器材摘要
Daylight 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 2024-08-30 under 510(k) number K233872. The device is classified under product code SCP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Daylight?
Daylight is a medical device that received FDA 510(k) clearance on 2024-08-30. The listed applicant is Big Health, Inc.. The 510(k) number is K233872.
When did Daylight receive FDA 510(k) clearance?
Daylight received FDA 510(k) clearance on 2024-08-30, under 510(k) number K233872.
Who is the listed applicant for Daylight?
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 Daylight?
The FDA product code for Daylight is SCP.
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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。
官方來源
在 FDA 資料庫中查看 →資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。
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