FDA 510(k)

Cios 連接

K 號：K153147 · 2016-01-12

決定日期2016-01-12

產品代碼OWB

諮詢委員會RA

決定相當於

器材摘要

Cios Connect is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2016-01-12 under 510(k) number K153147. The device is classified under product code OWB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Cios Connect?

Cios Connect is a medical device that received FDA 510(k) clearance on 2016-01-12. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K153147.

When did Cios Connect receive FDA 510(k) clearance?

Cios Connect received FDA 510(k) clearance on 2016-01-12, under 510(k) number K153147.

Who is the listed applicant for Cios Connect?

FDA 510(k) 記錄將西门子醫療解決方案美國，股份有限公司列為申請人。這並不單獨確立設備製造商。

What is the FDA product code for Cios Connect?

The FDA product code for Cios Connect is OWB.

其他以 Siemens Medical Solutions USA, 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。

K260055syngo.CT 脑量化 K261696ACUNAV Luxera 4D ICE 絲膜燒灼器 K260488MULTIX 震擊；MULTIX 震擊 C K253786syngo.CT 心臟駕駛艙 K253678MAMMOMAT B.閃耀 (11372950)K260844ACUSON Sequoia 診斷超聲系統;ACUSON Sequoia Select 診斷超聲系統;ACUSON Origin 診斷超聲系統;ACUSON Origin ICE 診斷超聲系統

查看所有 254 項裝置 →

相關器械（代碼：OWB）

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。

K253726uAngio AVIVA CXShanghai United Imaging Healthcare Co., Ltd.K261413EXTRON 3;EXTRON 6DRTECH Corporation K254205Zenition 30Philips Medical Systems Nederland B.V.K260607防護系統（西門子 30x40）Radiaction , Ltd.K253670SmartCT (R3.0 (L10))Philips Medical Systems B.V.K252735C-beamPulmera, Inc.

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。