FDA 510(k)

植入式電流雙極頭系統

K 號：K191569 · 2019-08-28

決定日期2019-08-28

產品代碼KWY

諮詢委員會或

決定相當於

器材摘要

Implantcast ic-Bipolar Head System is the device name listed in this FDA 510(k) record. The listed applicant is Implantcast GmbH. It received FDA 510(k) clearance on 2019-08-28 under 510(k) number K191569. The device is classified under product code KWY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Implantcast ic-Bipolar Head System?

Implantcast ic-Bipolar Head System is a medical device that received FDA 510(k) clearance on 2019-08-28. The listed applicant is Implantcast GmbH. The 510(k) number is K191569.

When did Implantcast ic-Bipolar Head System receive FDA 510(k) clearance?

Implantcast ic-Bipolar Head System received FDA 510(k) clearance on 2019-08-28, under 510(k) number K191569.

Who is the listed applicant for Implantcast ic-Bipolar Head System?

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

What is the FDA product code for Implantcast ic-Bipolar Head System?

The FDA product code for Implantcast ic-Bipolar Head System is KWY.

其他以 Implantcast GmbH 為申請人之記錄

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相關器械（代碼：KWY）

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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