FDA 510(k)

ストラウス・サーカル・膀胱鏡、子宮鏡およびアクセサリー機器

K番号: K260271 · 2026-03-27

決定日2026-03-27

製品コードFAJ

諮問委員会以下は、指定された医療機器規制テキストの日本語訳です。以下の医療機器規制テキストを日本語に翻訳してください。会社名、製品名、FDA、510(k)、PMA、NCT、PMID、識別子、およびURLを保護してください。ポリシー：medical-regulatory-v1 [原文] GU [翻訳] GU

決定大幅同等

医療機器の概要

Strauss Surgical cystoscope, hysteroscope and accessories 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 2026-03-27 under 510(k) number K260271. The device is classified under product code FAJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Strauss Surgical cystoscope, hysteroscope and accessories Instruments?

Strauss Surgical cystoscope, hysteroscope and accessories Instruments is a medical device that received FDA 510(k) clearance on 2026-03-27. The listed applicant is American Medical Endoscopy, Inc.. The 510(k) number is K260271.

When did Strauss Surgical cystoscope, hysteroscope and accessories Instruments receive FDA 510(k) clearance?

Strauss Surgical cystoscope, hysteroscope and accessories Instruments received FDA 510(k) clearance on 2026-03-27, under 510(k) number K260271.

Who is the listed applicant for Strauss Surgical cystoscope, hysteroscope and accessories 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 cystoscope, hysteroscope and accessories Instruments?

The FDA product code for Strauss Surgical cystoscope, hysteroscope and accessories Instruments is FAJ.

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

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。