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FDA 510(k)

Lux HD 檢測器,DRX-LC 檢測器,DRX-Revolution 移動 X 光系統

K 號:K253185 · 2026-03-11

決定日期2026-03-11
產品代碼IZL
諮詢委員會RA
決定相當於

器材摘要

Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray System is the device name listed in this FDA 510(k) record. The listed applicant is Carestream Health. It received FDA 510(k) clearance on 2026-03-11 under 510(k) number K253185. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray System?

Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray System is a medical device that received FDA 510(k) clearance on 2026-03-11. The listed applicant is Carestream Health. The 510(k) number is K253185.

When did Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray System receive FDA 510(k) clearance?

Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray System received FDA 510(k) clearance on 2026-03-11, under 510(k) number K253185.

Who is the listed applicant for Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray System?

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

What is the FDA product code for Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray System?

The FDA product code for Lux HD Detectors, DRX-LC Detector, DRX-Revolution Mobile X-Ray System is IZL.

相關臨床試驗

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其他以 Carestream Health 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:IZL)

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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