FDA 510(k)

K-ASSAY CRP (版本2)

K 號：K242170 · 2025-04-18

決定日期2025-04-18

產品代碼DCK

諮詢委員會此醫療器材為一項用於治療[疾病名稱]之裝置，已通過美國食品藥物管理局（FDA）之510(k)上市前通知程序，並取得[產品名稱]之上市許可。本裝置亦已獲得PMA（上市前核准）之認可，相關臨床試驗資料已登錄於ClinicalTrials.gov（NCT編號：[NCT號碼]），並已發表於經同儕審查之醫學期刊（PMID：[PMID號碼]）。更多詳細資訊請參閱：[URL]。

決定相當於

器材摘要

K-ASSAY CRP (Ver.2) is the device name listed in this FDA 510(k) record. The listed applicant is Kamiya Biomedical Company, LLC. It received FDA 510(k) clearance on 2025-04-18 under 510(k) number K242170. The device is classified under product code DCK. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the K-ASSAY CRP (Ver.2)?

K-ASSAY CRP (Ver.2) is a medical device that received FDA 510(k) clearance on 2025-04-18. The listed applicant is Kamiya Biomedical Company, LLC. The 510(k) number is K242170.

When did K-ASSAY CRP (Ver.2) receive FDA 510(k) clearance?

K-ASSAY CRP (Ver.2) received FDA 510(k) clearance on 2025-04-18, under 510(k) number K242170.

Who is the listed applicant for K-ASSAY CRP (Ver.2)?

The FDA 510(k) record lists Kamiya Biomedical Company, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for K-ASSAY CRP (Ver.2)?

The FDA product code for K-ASSAY CRP (Ver.2) is DCK.

相關器械（代碼：DCK）

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

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