FDA 510(k)

ECHELON ENDOPATH Staple Line Reinforcement (ECH60R)

K番号: K252906 · 2026-01-09

決定日2026-01-09

製品コードOXC

諮問委員会SU

決定Substantially Equivalent

医療機器の概要

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.

よくある質問

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)?

The FDA 510(k) record lists Ethicon Endo-Surgery, LLC as the applicant. This does not by itself establish the device manufacturer.

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.

申請者としてEthicon Endo-Surgery, LLCを記載するその他の記録

すべての35件のデバイスを表示 →

公式ソース

FDAデータベースで見る →

データはFDA Open APIから取得しています。最新かつ権威ある情報については、常に公式レコードを参照してください。