FDA 510(k)

ポータブルDR画像システム

K番号: K253058 · 2026-06-18

申請者Shantou Institute of Ultrasonic Instruments Co., Ltd.

決定日2026-06-18

製品コードIZL

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

Portable DR Imaging System is the device name listed in this FDA 510(k) record. The listed applicant is Shantou Institute of Ultrasonic Instruments Co., Ltd.. It received FDA 510(k) clearance on 2026-06-18 under 510(k) number K253058. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

よくある質問

What is the Portable DR Imaging System?

Portable DR Imaging System is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is Shantou Institute of Ultrasonic Instruments Co., Ltd.. The 510(k) number is K253058.

When did Portable DR Imaging System receive FDA 510(k) clearance?

Portable DR Imaging System received FDA 510(k) clearance on 2026-06-18, under 510(k) number K253058.

Who is the listed applicant for Portable DR Imaging System?

The FDA 510(k) record lists Shantou Institute of Ultrasonic Instruments Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Portable DR Imaging System?

The FDA product code for Portable DR Imaging System is IZL.

申請者としてShantou Institute of Ultrasonic Instruments Co., Ltd.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。