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FDA 510(k)

MiPACS HTML5 網頁檢視器

K 號：K212984 · 2021-11-12

申請人Lead Technologies, Inc.
決定日期2021-11-12
產品代碼LLZ
諮詢委員會RA
決定相當於

器材摘要

MiPACS HTML5 Web Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Lead Technologies, Inc.. It received FDA 510(k) clearance on 2021-11-12 under 510(k) number K212984. 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 MiPACS HTML5 Web Viewer?

MiPACS HTML5 Web Viewer is a medical device that received FDA 510(k) clearance on 2021-11-12. The listed applicant is Lead Technologies, Inc.. The 510(k) number is K212984.

When did MiPACS HTML5 Web Viewer receive FDA 510(k) clearance?

MiPACS HTML5 Web Viewer received FDA 510(k) clearance on 2021-11-12, under 510(k) number K212984.

Who is the listed applicant for MiPACS HTML5 Web Viewer?

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

What is the FDA product code for MiPACS HTML5 Web Viewer?

The FDA product code for MiPACS HTML5 Web Viewer is LLZ.

相關臨床試驗

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：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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