FDA 510(k)

歐里恩生命週期 MEG

K 號：K191785 · 2020-02-14

決定日期2020-02-14

產品代碼OLY

諮詢委員會NE (請提供完整的英文描述，以便進行翻譯。)

決定相當於

器材摘要

Orion LifeSpan MEG is the device name listed in this FDA 510(k) record. The listed applicant is Compumedics Limited. It received FDA 510(k) clearance on 2020-02-14 under 510(k) number K191785. The device is classified under product code OLY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Orion LifeSpan MEG?

Orion LifeSpan MEG is a medical device that received FDA 510(k) clearance on 2020-02-14. The listed applicant is Compumedics Limited. The 510(k) number is K191785.

When did Orion LifeSpan MEG receive FDA 510(k) clearance?

Orion LifeSpan MEG received FDA 510(k) clearance on 2020-02-14, under 510(k) number K191785.

Who is the listed applicant for Orion LifeSpan MEG?

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

What is the FDA product code for Orion LifeSpan MEG?

The FDA product code for Orion LifeSpan MEG is OLY.

其他以 Compumedics Limited 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。

K252383Somfit D K242447Falcon HST K231546Somfit K230073Okti

相關器械（代碼：OLY）

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。

K152184MagView 生物磁力計系統Tristan Technologies, Inc.

官方來源

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