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FDA 510(k)

Kurin血液培養收集套件,配備Kurin鎖定技術

K 號:K220677 · 2023-04-28

申請人Kurin, Inc.
決定日期2023-04-28
產品代碼JKA
諮詢委員會CH
決定相當於

器材摘要

Kurin Blood Culture Collection Set with Kurin Lock Technology is the device name listed in this FDA 510(k) record. The listed applicant is Kurin, Inc.. It received FDA 510(k) clearance on 2023-04-28 under 510(k) number K220677. 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 Kurin Blood Culture Collection Set with Kurin Lock Technology?

Kurin Blood Culture Collection Set with Kurin Lock Technology is a medical device that received FDA 510(k) clearance on 2023-04-28. The listed applicant is Kurin, Inc.. The 510(k) number is K220677.

When did Kurin Blood Culture Collection Set with Kurin Lock Technology receive FDA 510(k) clearance?

Kurin Blood Culture Collection Set with Kurin Lock Technology received FDA 510(k) clearance on 2023-04-28, under 510(k) number K220677.

Who is the listed applicant for Kurin Blood Culture Collection Set with Kurin Lock Technology?

The FDA 510(k) record lists Kurin, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Kurin Blood Culture Collection Set with Kurin Lock Technology?

The FDA product code for Kurin Blood Culture Collection Set with Kurin Lock Technology is JKA.

相關臨床試驗

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。

其他以 Kurin, 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。

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。

官方來源

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