LifeOutcomes C-Quest™ 體液培養採樣設備
K 號：K231282 · 2024-01-26
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器材摘要
LifeOutcomes C-Quest™ Blood Culture Sampling Device is the device name listed in this FDA 510(k) record. The listed applicant is Lifeoutcomes, LLC. It received FDA 510(k) clearance on 2024-01-26 under 510(k) number K231282. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.
常見問題
What is the LifeOutcomes C-Quest™ Blood Culture Sampling Device?
LifeOutcomes C-Quest™ Blood Culture Sampling Device is a medical device that received FDA 510(k) clearance on 2024-01-26. The listed applicant is Lifeoutcomes, LLC. The 510(k) number is K231282.
When did LifeOutcomes C-Quest™ Blood Culture Sampling Device receive FDA 510(k) clearance?
LifeOutcomes C-Quest™ Blood Culture Sampling Device received FDA 510(k) clearance on 2024-01-26, under 510(k) number K231282.
Who is the listed applicant for LifeOutcomes C-Quest™ Blood Culture Sampling Device?
The FDA 510(k) record lists Lifeoutcomes, LLC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LifeOutcomes C-Quest™ Blood Culture Sampling Device?
The FDA product code for LifeOutcomes C-Quest™ Blood Culture Sampling Device is JKA.
相關臨床試驗
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相關器械（代碼：JKA）
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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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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