FDA 510(k)

mediCAD 4.0

K 號：K170702 · 2018-09-07

決定日期2018-09-07

產品代碼LLZ

諮詢委員會RA

決定相當於

器材摘要

mediCAD 4.0 is the device name listed in this FDA 510(k) record. The listed applicant is Medicad Hectec GmbH. It received FDA 510(k) clearance on 2018-09-07 under 510(k) number K170702. 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 mediCAD 4.0?

mediCAD 4.0 is a medical device that received FDA 510(k) clearance on 2018-09-07. The listed applicant is Medicad Hectec GmbH. The 510(k) number is K170702.

When did mediCAD 4.0 receive FDA 510(k) clearance?

mediCAD 4.0 received FDA 510(k) clearance on 2018-09-07, under 510(k) number K170702.

Who is the listed applicant for mediCAD 4.0?

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

What is the FDA product code for mediCAD 4.0?

The FDA product code for mediCAD 4.0 is LLZ.

其他以 Medicad Hectec GmbH 為申請人之記錄

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K183412mediCAD 網絡

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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