FDA 510(k)

ASAHI Corsair Armet

K-Number: K152249 · 2016-03-04

Decision Date2016-03-04

Product CodeDQY

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

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

Frequently Asked Questions

What is the ASAHI Corsair Armet?

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

When was ASAHI Corsair Armet approved by the FDA?

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

What company makes ASAHI Corsair Armet?

ASAHI Corsair Armet is manufactured by Asahi Intecc Co., Ltd..

What is the FDA product code for ASAHI Corsair Armet?

The FDA product code for ASAHI Corsair Armet is DQY.

Other Devices by Asahi Intecc Co., Ltd.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.