王儀血液採集套組
K 號：K232308 · 2023-12-04
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器材摘要
Monarch Blood Collection Set is the device name listed in this FDA 510(k) record. The listed applicant is The Monarch Company. It received FDA 510(k) clearance on 2023-12-04 under 510(k) number K232308. 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 Monarch Blood Collection Set?
Monarch Blood Collection Set is a medical device that received FDA 510(k) clearance on 2023-12-04. The listed applicant is The Monarch Company. The 510(k) number is K232308.
When did Monarch Blood Collection Set receive FDA 510(k) clearance?
Monarch Blood Collection Set received FDA 510(k) clearance on 2023-12-04, under 510(k) number K232308.
Who is the listed applicant for Monarch Blood Collection Set?
The FDA 510(k) record lists The Monarch Company as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Monarch Blood Collection Set?
The FDA product code for Monarch Blood Collection Set is JKA.
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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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