FDA 510(k)

飛利浦 MR 病患照護入口網站

K 號：K212227 · 2021-09-30

決定日期2021-09-30

產品代碼MWI

諮詢委員會履歷

決定相當於

器材摘要

Philips MR Patient Care Portal is the device name listed in this FDA 510(k) record. The listed applicant is Invivo Corporation. It received FDA 510(k) clearance on 2021-09-30 under 510(k) number K212227. The device is classified under product code MWI. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Philips MR Patient Care Portal?

Philips MR Patient Care Portal is a medical device that received FDA 510(k) clearance on 2021-09-30. The listed applicant is Invivo Corporation. The 510(k) number is K212227.

When did Philips MR Patient Care Portal receive FDA 510(k) clearance?

Philips MR Patient Care Portal received FDA 510(k) clearance on 2021-09-30, under 510(k) number K212227.

Who is the listed applicant for Philips MR Patient Care Portal?

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

What is the FDA product code for Philips MR Patient Care Portal?

The FDA product code for Philips MR Patient Care Portal is MWI.

其他以 Invivo Corporation 為申請人之記錄

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相關器械（代碼：MWI）

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。

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