FDA 510(k)

ECHELON ENDOPATH 鍵線強化器 (ECH60R)

K 號：K252906 · 2026-01-09

決定日期2026-01-09

產品代碼OXC

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

ECHELON ENDOPATH Staple Line Reinforcement (ECH60R) is the device name listed in this FDA 510(k) record. The listed applicant is Ethicon Endo-Surgery, LLC. It received FDA 510(k) clearance on 2026-01-09 under 510(k) number K252906. The device is classified under product code OXC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ECHELON ENDOPATH Staple Line Reinforcement (ECH60R)?

ECHELON ENDOPATH Staple Line Reinforcement (ECH60R) is a medical device that received FDA 510(k) clearance on 2026-01-09. The listed applicant is Ethicon Endo-Surgery, LLC. The 510(k) number is K252906.

When did ECHELON ENDOPATH Staple Line Reinforcement (ECH60R) receive FDA 510(k) clearance?

ECHELON ENDOPATH Staple Line Reinforcement (ECH60R) received FDA 510(k) clearance on 2026-01-09, under 510(k) number K252906.

Who is the listed applicant for ECHELON ENDOPATH Staple Line Reinforcement (ECH60R)?

FDA 510(k) 記錄中將 Ethicon Endo-Surgery, LLC 列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for ECHELON ENDOPATH Staple Line Reinforcement (ECH60R)?

The FDA product code for ECHELON ENDOPATH Staple Line Reinforcement (ECH60R) is OXC.

其他以 Ethicon Endo-Surgery, LLC 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。

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相關器械（代碼：OXC）

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。

K231603標準釘線強化（SSLR23）Standard Bariatrics, Inc.K221343ECHELON ENDOPATH 鍵線強化器Ethicon Endo-Surgery, LLC K221487NEOVEIL 鋼釘線加固Gunze Limited K190937Echelon Endopath 粘合線強化設備Ethicon Endo-Surgery, LLC K181940GORE SEAMGUARD 生物可吸收釘線強化材W. L. Gore & Associates, Inc.

官方來源

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