FDA 510(k)

スマートサージナービジョナリーシステム

K番号: K242163 · 2026-04-20

決定日2026-04-20

製品コードOWN

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

SmartSurgN Visualization System is the device name listed in this FDA 510(k) record. The listed applicant is SmartsurgN, Inc.. It received FDA 510(k) clearance on 2026-04-20 under 510(k) number K242163. The device is classified under product code OWN. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the SmartSurgN Visualization System?

SmartSurgN Visualization System is a medical device that received FDA 510(k) clearance on 2026-04-20. The listed applicant is SmartsurgN, Inc.. The 510(k) number is K242163.

When did SmartSurgN Visualization System receive FDA 510(k) clearance?

SmartSurgN Visualization System received FDA 510(k) clearance on 2026-04-20, under 510(k) number K242163.

Who is the listed applicant for SmartSurgN Visualization System?

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

What is the FDA product code for SmartSurgN Visualization System?

The FDA product code for SmartSurgN Visualization System is OWN.

申請者としてSmartsurgN, Inc.を記載するその他の記録

K242772AirSurgN Insufflator (10030/AirSurgN)

公式ソース

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