FDA 510(k)

ヴィーナス・アンリミテッド・デュアル、ヴィーナス・アンリミテッド・ヒペア、ヴィーナス・アンリミテッド・ウロ・診断超音波システム

K番号: K243298 · 2025-04-03

申請者Carbon (Shenzhen) Medical Device Co., Ltd.

決定日2025-04-03

製品コードIYN

諮問委員会RA （注：由于原文中未提供具体的医疗设备监管文本内容，因此无法进行翻译。请提供具体的文本内容以便进行翻译。）

決定大幅同等

医療機器の概要

Venus Ultimate-Dual, Venus Ultimate-Hepa, Venus Ultimate-Uro Diagnostic Ultrasound System is the device name listed in this FDA 510(k) record. The listed applicant is Carbon (Shenzhen) Medical Device Co., Ltd.. It received FDA 510(k) clearance on 2025-04-03 under 510(k) number K243298. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Venus Ultimate-Dual, Venus Ultimate-Hepa, Venus Ultimate-Uro Diagnostic Ultrasound System?

Venus Ultimate-Dual, Venus Ultimate-Hepa, Venus Ultimate-Uro Diagnostic Ultrasound System is a medical device that received FDA 510(k) clearance on 2025-04-03. The listed applicant is Carbon (Shenzhen) Medical Device Co., Ltd.. The 510(k) number is K243298.

When did Venus Ultimate-Dual, Venus Ultimate-Hepa, Venus Ultimate-Uro Diagnostic Ultrasound System receive FDA 510(k) clearance?

Venus Ultimate-Dual, Venus Ultimate-Hepa, Venus Ultimate-Uro Diagnostic Ultrasound System received FDA 510(k) clearance on 2025-04-03, under 510(k) number K243298.

Who is the listed applicant for Venus Ultimate-Dual, Venus Ultimate-Hepa, Venus Ultimate-Uro Diagnostic Ultrasound System?

The FDA 510(k) record lists Carbon (Shenzhen) Medical Device Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Venus Ultimate-Dual, Venus Ultimate-Hepa, Venus Ultimate-Uro Diagnostic Ultrasound System?

The FDA product code for Venus Ultimate-Dual, Venus Ultimate-Hepa, Venus Ultimate-Uro Diagnostic Ultrasound System is IYN.

申請者としてCarbon (Shenzhen) Medical Device Co., Ltd.を記載するその他の記録

K243296disposableバイオプシー針

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