Spectrum 唾液收集器
K 號：K223497 · 2023-02-17
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器材摘要
Spectrum Saliva Collection Device is the device name listed in this FDA 510(k) record. The listed applicant is Spectrum Solutions, LLC. It received FDA 510(k) clearance on 2023-02-17 under 510(k) number K223497. The device is classified under product code QBD. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the Spectrum Saliva Collection Device?
Spectrum Saliva Collection Device is a medical device that received FDA 510(k) clearance on 2023-02-17. The listed applicant is Spectrum Solutions, LLC. The 510(k) number is K223497.
When did Spectrum Saliva Collection Device receive FDA 510(k) clearance?
Spectrum Saliva Collection Device received FDA 510(k) clearance on 2023-02-17, under 510(k) number K223497.
Who is the listed applicant for Spectrum Saliva Collection Device?
The FDA 510(k) record lists Spectrum Solutions, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Spectrum Saliva Collection Device?
The FDA product code for Spectrum Saliva Collection Device is QBD.
相關臨床試驗
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相關器械（代碼：QBD）
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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