FDA 510(k)

Penumbra 智能電纜

K 號：K160832 · 2016-04-20

決定日期2016-04-20

產品代碼HCG

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

Penumbra Smart Coil is the device name listed in this FDA 510(k) record. The listed applicant is Penumbra, Inc.. It received FDA 510(k) clearance on 2016-04-20 under 510(k) number K160832. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Penumbra Smart Coil?

Penumbra Smart Coil is a medical device that received FDA 510(k) clearance on 2016-04-20. The listed applicant is Penumbra, Inc.. The 510(k) number is K160832.

When did Penumbra Smart Coil receive FDA 510(k) clearance?

Penumbra Smart Coil received FDA 510(k) clearance on 2016-04-20, under 510(k) number K160832.

Who is the listed applicant for Penumbra Smart Coil?

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

What is the FDA product code for Penumbra Smart Coil?

The FDA product code for Penumbra Smart Coil is HCG.

其他以 Penumbra, Inc. 為申請人之記錄

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K250690Penumbra 系統（Thunderbolt 吸引管）K260599INDIGO® 吸引系統 – INDIGO 鏈接 K251949INDIGO® 吸引系統 - 雷電閃吸管連結版 K252612INDIGO® 吸引系統 – 雷電閃吸管；INDIGO® 吸引系統 – 雷電閃吸管 K250079Ruby XL 系統 K242104Penumbra 系統（再灌流導管 RED 72）

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相關器械（代碼：HCG）

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