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FDA 510(k)

卡迪那爾健康™多層加強外科袍

K 號:K253243 · 2026-04-28

決定日期2026-04-28
產品代碼FYA
諮詢委員會SU 請提供完整的描述文本,以便我進行翻譯。
決定相當於

器材摘要

Cardinal Health™ Poly Reinforced Surgical Gown is the device name listed in this FDA 510(k) record. The listed applicant is Cardinal Health 200, LLC. It received FDA 510(k) clearance on 2026-04-28 under 510(k) number K253243. The device is classified under product code FYA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Cardinal Health™ Poly Reinforced Surgical Gown?

Cardinal Health™ Poly Reinforced Surgical Gown is a medical device that received FDA 510(k) clearance on 2026-04-28. The listed applicant is Cardinal Health 200, LLC. The 510(k) number is K253243.

When did Cardinal Health™ Poly Reinforced Surgical Gown receive FDA 510(k) clearance?

Cardinal Health™ Poly Reinforced Surgical Gown received FDA 510(k) clearance on 2026-04-28, under 510(k) number K253243.

Who is the listed applicant for Cardinal Health™ Poly Reinforced Surgical Gown?

The FDA 510(k) record lists Cardinal Health 200, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cardinal Health™ Poly Reinforced Surgical Gown?

The FDA product code for Cardinal Health™ Poly Reinforced Surgical Gown is FYA.

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。

相關器械(代碼:FYA)

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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