FDA 510(k)

MOSAIQ 癌症資訊系統

K 號：K183034 · 2018-12-04

決定日期2018-12-04

產品代碼IYE

諮詢委員會RA

決定相當於

器材摘要

MOSAIQ Oncology Information System is the device name listed in this FDA 510(k) record. The listed applicant is Elekta, Inc.. It received FDA 510(k) clearance on 2018-12-04 under 510(k) number K183034. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the MOSAIQ Oncology Information System?

MOSAIQ Oncology Information System is a medical device that received FDA 510(k) clearance on 2018-12-04. The listed applicant is Elekta, Inc.. The 510(k) number is K183034.

When did MOSAIQ Oncology Information System receive FDA 510(k) clearance?

MOSAIQ Oncology Information System received FDA 510(k) clearance on 2018-12-04, under 510(k) number K183034.

Who is the listed applicant for MOSAIQ Oncology Information System?

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

What is the FDA product code for MOSAIQ Oncology Information System?

The FDA product code for MOSAIQ Oncology Information System is IYE.

其他以 Elekta, 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。

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相關器械（代碼：IYE）

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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