FDA 510(k)

Alegria Flash CTD屏幕

K 號：K250666 · 2025-10-22

決定日期2025-10-22

產品代碼LLL

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

Alegria Flash CTD Screen is the device name listed in this FDA 510(k) record. The listed applicant is Zeus Scientific. It received FDA 510(k) clearance on 2025-10-22 under 510(k) number K250666. The device is classified under product code LLL. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Alegria Flash CTD Screen?

Alegria Flash CTD Screen is a medical device that received FDA 510(k) clearance on 2025-10-22. The listed applicant is Zeus Scientific. The 510(k) number is K250666.

When did Alegria Flash CTD Screen receive FDA 510(k) clearance?

Alegria Flash CTD Screen received FDA 510(k) clearance on 2025-10-22, under 510(k) number K250666.

Who is the listed applicant for Alegria Flash CTD Screen?

FDA 510(k) 記錄將宙斯科學列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Alegria Flash CTD Screen?

The FDA product code for Alegria Flash CTD Screen is LLL.