CLEARinse CTS 样本收集及運輸系統
K 號：K221664 · 2023-07-03
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器材摘要
CLEARinse CTS Specimen Collection and Transport System is the device name listed in this FDA 510(k) record. The listed applicant is Aardvark Medical, Inc.. It received FDA 510(k) clearance on 2023-07-03 under 510(k) number K221664. 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 CLEARinse CTS Specimen Collection and Transport System?
CLEARinse CTS Specimen Collection and Transport System is a medical device that received FDA 510(k) clearance on 2023-07-03. The listed applicant is Aardvark Medical, Inc.. The 510(k) number is K221664.
When did CLEARinse CTS Specimen Collection and Transport System receive FDA 510(k) clearance?
CLEARinse CTS Specimen Collection and Transport System received FDA 510(k) clearance on 2023-07-03, under 510(k) number K221664.
Who is the listed applicant for CLEARinse CTS Specimen Collection and Transport System?
The FDA 510(k) record lists Aardvark Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLEARinse CTS Specimen Collection and Transport System?
The FDA product code for CLEARinse CTS Specimen Collection and Transport System is QBD.
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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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