FDA 510(k)

Cydar EV (系列B) 及 Cydar EV 地圖

K 號：K212442 · 2021-12-03

決定日期2021-12-03

產品代碼OWB

諮詢委員會RA

決定相當於

器材摘要

Cydar EV (Series B) and Cydar EV Maps is the device name listed in this FDA 510(k) record. The listed applicant is Cydar , Ltd.. It received FDA 510(k) clearance on 2021-12-03 under 510(k) number K212442. 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 Cydar EV (Series B) and Cydar EV Maps?

Cydar EV (Series B) and Cydar EV Maps is a medical device that received FDA 510(k) clearance on 2021-12-03. The listed applicant is Cydar , Ltd.. The 510(k) number is K212442.

When did Cydar EV (Series B) and Cydar EV Maps receive FDA 510(k) clearance?

Cydar EV (Series B) and Cydar EV Maps received FDA 510(k) clearance on 2021-12-03, under 510(k) number K212442.

Who is the listed applicant for Cydar EV (Series B) and Cydar EV Maps?

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

What is the FDA product code for Cydar EV (Series B) and Cydar EV Maps?

The FDA product code for Cydar EV (Series B) and Cydar EV Maps is OWB.

其他以 Cydar , Ltd. 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。

K160088Cydar EV

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。