FDA 510(k)

ASAHI Corsair Armet

K 號：K152249 · 2016-03-04

決定日期2016-03-04

產品代碼DQY

諮詢委員會履歷

決定相當於

器材摘要

ASAHI Corsair Armet is the device name listed in this FDA 510(k) record. The listed applicant is Asahi Intecc Co., Ltd.. It received FDA 510(k) clearance on 2016-03-04 under 510(k) number K152249. The device is classified under product code DQY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the ASAHI Corsair Armet?

ASAHI Corsair Armet is a medical device that received FDA 510(k) clearance on 2016-03-04. The listed applicant is Asahi Intecc Co., Ltd.. The 510(k) number is K152249.

When did ASAHI Corsair Armet receive FDA 510(k) clearance?

ASAHI Corsair Armet received FDA 510(k) clearance on 2016-03-04, under 510(k) number K152249.

Who is the listed applicant for ASAHI Corsair Armet?

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

What is the FDA product code for ASAHI Corsair Armet?

The FDA product code for ASAHI Corsair Armet is DQY.

其他以 Asahi Intecc Co., Ltd. 為申請人之記錄

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