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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 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 2018-12-20 under 510(k) 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. The listed applicant is Asahi Intecc Co., Ltd.. The 510(k) number is K182420.

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

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

Who is the listed applicant for ASAHI Corsair Pro XS?

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 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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