FDA 510(k)

感應式深度電極

K 號：K213170 · 2023-04-18

決定日期2023-04-18

產品代碼GZL

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

SENSOSEEG Depth Electrodes is the device name listed in this FDA 510(k) record. The listed applicant is Sensomedical Labs, Ltd.. It received FDA 510(k) clearance on 2023-04-18 under 510(k) number K213170. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the SENSOSEEG Depth Electrodes?

SENSOSEEG Depth Electrodes is a medical device that received FDA 510(k) clearance on 2023-04-18. The listed applicant is Sensomedical Labs, Ltd.. The 510(k) number is K213170.

When did SENSOSEEG Depth Electrodes receive FDA 510(k) clearance?

SENSOSEEG Depth Electrodes received FDA 510(k) clearance on 2023-04-18, under 510(k) number K213170.

Who is the listed applicant for SENSOSEEG Depth Electrodes?

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

What is the FDA product code for SENSOSEEG Depth Electrodes?

The FDA product code for SENSOSEEG Depth Electrodes is GZL.

其他以 Sensomedical Labs, Ltd. 為申請人之記錄

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K253970沃威恩深度電極

相關器械（代碼：GZL）

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官方來源

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