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FDA 510(k)

ASAHI Corsair Pro XS

K-Number: K182420 · 2018-12-20

ApplicantAsahi Intecc Co., Ltd.
Decision Date2018-12-20
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ASAHI Corsair Pro XS is a medical device manufactured by Asahi Intecc Co., Ltd.. It received FDA 510(k) clearance on 2018-12-20 under approval number K182420. 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 Pro XS?

ASAHI Corsair Pro XS is a medical device that received FDA 510(k) clearance on 2018-12-20. It is manufactured by Asahi Intecc Co., Ltd.. The 510(k) number is K182420.

When was ASAHI Corsair Pro XS approved by the FDA?

ASAHI Corsair Pro XS received FDA 510(k) clearance on 2018-12-20, under approval number K182420.

What company makes ASAHI Corsair Pro XS?

ASAHI Corsair Pro XS is manufactured by Asahi Intecc Co., Ltd..

What is the FDA product code for ASAHI Corsair Pro XS?

The FDA product code for ASAHI Corsair Pro XS is DQY.

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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.

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