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FDA 510(k)

ASAHI CORSAIR MICROCATHETER

K-Number: K083127 · 2009-02-03

ApplicantAsahi Intecc Co., Ltd.
Decision Date2009-02-03
Product CodeDQY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ASAHI CORSAIR MICROCATHETER 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 2009-02-03 under 510(k) number K083127. 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 MICROCATHETER?

ASAHI CORSAIR MICROCATHETER is a medical device that received FDA 510(k) clearance on 2009-02-03. The listed applicant is Asahi Intecc Co., Ltd.. The 510(k) number is K083127.

When did ASAHI CORSAIR MICROCATHETER receive FDA 510(k) clearance?

ASAHI CORSAIR MICROCATHETER received FDA 510(k) clearance on 2009-02-03, under 510(k) number K083127.

Who is the listed applicant for ASAHI CORSAIR MICROCATHETER?

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 MICROCATHETER?

The FDA product code for ASAHI CORSAIR MICROCATHETER 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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