FDA 510(k)

ストラス surgical切除器具

K番号: K253020 · 2026-06-04

決定日2026-06-04

製品コードHIH

諮問委員会医薬品機器規制テキストの翻訳は以下の通りです。 [原文] OB [翻訳] OB

決定大幅同等

医療機器の概要

Strauss Surgical Resection Instruments is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Endoscopy, Inc.. It received FDA 510(k) clearance on 2026-06-04 under 510(k) number K253020. The device is classified under product code HIH. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Strauss Surgical Resection Instruments?

Strauss Surgical Resection Instruments is a medical device that received FDA 510(k) clearance on 2026-06-04. The listed applicant is American Medical Endoscopy, Inc.. The 510(k) number is K253020.

When did Strauss Surgical Resection Instruments receive FDA 510(k) clearance?

Strauss Surgical Resection Instruments received FDA 510(k) clearance on 2026-06-04, under 510(k) number K253020.

Who is the listed applicant for Strauss Surgical Resection Instruments?

The FDA 510(k) record lists American Medical Endoscopy, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Strauss Surgical Resection Instruments?

The FDA product code for Strauss Surgical Resection Instruments is HIH.

申請者としてAmerican Medical Endoscopy, Inc.を記載するその他の記録

公式ソース

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