FDA 510(k)

腦光醫療設備

K 號：K202808 · 2021-10-14

申請人Advantis Medical Imaging Single Member P.C.

決定日期2021-10-14

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

Brainance MD is the device name listed in this FDA 510(k) record. The listed applicant is Advantis Medical Imaging Single Member P.C.. It received FDA 510(k) clearance on 2021-10-14 under 510(k) number K202808. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Brainance MD?

Brainance MD is a medical device that received FDA 510(k) clearance on 2021-10-14. The listed applicant is Advantis Medical Imaging Single Member P.C.. The 510(k) number is K202808.

When did Brainance MD receive FDA 510(k) clearance?

Brainance MD received FDA 510(k) clearance on 2021-10-14, under 510(k) number K202808.

Who is the listed applicant for Brainance MD?

The FDA 510(k) record lists Advantis Medical Imaging Single Member P.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Brainance MD?

The FDA product code for Brainance MD is LLZ.

其他以 Advantis Medical Imaging Single Member P.C. 為申請人之記錄

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K222975Advantis 平臺

相關器械（代碼：LLZ）

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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官方來源

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