FDA 510(k)

SKOUT®系統

K 號：K240781 · 2024-04-19

決定日期2024-04-19

產品代碼QNP

諮詢委員會GU

決定相當於

器材摘要

SKOUT® system is the device name listed in this FDA 510(k) record. The listed applicant is Iterative Scopes, Inc.. It received FDA 510(k) clearance on 2024-04-19 under 510(k) number K240781. The device is classified under product code QNP. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the SKOUT® system?

SKOUT® system is a medical device that received FDA 510(k) clearance on 2024-04-19. The listed applicant is Iterative Scopes, Inc.. The 510(k) number is K240781.

When did SKOUT® system receive FDA 510(k) clearance?

SKOUT® system received FDA 510(k) clearance on 2024-04-19, under 510(k) number K240781.

Who is the listed applicant for SKOUT® system?

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

What is the FDA product code for SKOUT® system?

The FDA product code for SKOUT® system is QNP.

其他以 Iterative Scopes, 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。

K241508SKOUT®系統 K230658SKOUT®系統 K213686SKOUT軟體

相關器械（代碼：QNP）

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。

K260133CADDIEOdin Medical Limited K260567EW10-EC02內視鏡輔助程序Fujifilm Corporation K252853CAD - 下消化道 (EC07-01)Xiamen Inno Medical Technology Co., Ltd.K261369GI Geniux™ 模組 300 (GGM300-US)；ColonPRO™ US (CPRO403S-US)Cosmo Artificial Intelligence - Ai, Ltd.K260724MAGENTIQ-COLO (ME-APDS)Magentiq Eye, Ltd.K253664SKOUT系統Iterative Health

官方來源

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