FDA 510(k)

iQFlex Pro

K 號：K240009 · 2024-07-03

決定日期2024-07-03

產品代碼IZL

諮詢委員會RA

決定相當於

器材摘要

iQFlex Pro is the device name listed in this FDA 510(k) record. The listed applicant is First Source, Inc.. It received FDA 510(k) clearance on 2024-07-03 under 510(k) number K240009. The device is classified under product code IZL. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the iQFlex Pro?

iQFlex Pro is a medical device that received FDA 510(k) clearance on 2024-07-03. The listed applicant is First Source, Inc.. The 510(k) number is K240009.

When did iQFlex Pro receive FDA 510(k) clearance?

iQFlex Pro received FDA 510(k) clearance on 2024-07-03, under 510(k) number K240009.

Who is the listed applicant for iQFlex Pro?

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

What is the FDA product code for iQFlex Pro?

The FDA product code for iQFlex Pro is IZL.

其他以 First Source, Inc. 為申請人之記錄

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

K221081iQFlex M 移動X光系統，iQFlex MD 移動X光系統 K203703I-Q 觀察

相關器械（代碼：IZL）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

K260236XLITEGEMSS HEALTHCARE CO., LTD.K253058攜帶式DR影像系統Shantou Institute of Ultrasonic Instruments Co., Ltd.K260085RAYMO移動X光系統（型號：RAYMO）DRGEM Corporation K253185Lux HD 檢測器，DRX-LC 檢測器，DRX-Revolution 移動 X 光系統Carestream Health K253244AirRay-mini 80A, AirRay-mini 90A, AirRay-mini 80F, AirRay-mini 90F (AirRay-mini)Poskom Co., Ltd.K250976Airbile-100Poskom Co., Ltd.

官方來源

在 FDA 資料庫中查看 →

資料來源為 FDA Open API。如需最新且權威的資訊，請始終參閱官方記錄。